U.S. patent application number 17/569929 was filed with the patent office on 2022-04-28 for glaucoma treatment devices and methods.
The applicant listed for this patent is MicroOptx Inc.. Invention is credited to J. David Brown, Edward Aaron Cohen, Roy Christian Martin, Christopher Clark Pulling.
Application Number | 20220125638 17/569929 |
Document ID | / |
Family ID | |
Filed Date | 2022-04-28 |
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United States Patent
Application |
20220125638 |
Kind Code |
A1 |
Brown; J. David ; et
al. |
April 28, 2022 |
GLAUCOMA TREATMENT DEVICES AND METHODS
Abstract
Devices can be implanted in an eye to treat glaucoma and/or dry
eye. The devices described herein include a body defining a lumen
and having first and second ends and external and lumenal surfaces.
The body has a length sufficient to provide fluid communication
between the anterior chamber and tear film of the eye through the
lumen when the device is implanted in the sclera. The body can
include a radiused distal edge. A distal end portion of the body
can be laterally flared. The body can include a mid-body portion
that is laterally narrower than distal and proximal end portions of
the body. Methods of treating glaucoma and/or dry eye, wherein the
device is implanted in the sclera of an afflicted eye, are also
described.
Inventors: |
Brown; J. David; (St. Paul,
MN) ; Pulling; Christopher Clark; (Dayton, MN)
; Martin; Roy Christian; (Maple Grove, MN) ;
Cohen; Edward Aaron; (Columbia Heights, MN) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
MicroOptx Inc. |
Maple Grove |
MN |
US |
|
|
Appl. No.: |
17/569929 |
Filed: |
January 6, 2022 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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16315499 |
Jan 4, 2019 |
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PCT/US2017/040738 |
Jul 5, 2017 |
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17569929 |
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62359044 |
Jul 6, 2016 |
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International
Class: |
A61F 9/007 20060101
A61F009/007; A61F 9/013 20060101 A61F009/013 |
Claims
1. A device for treating an eye, the device comprising: a body
having a distal end portion, a mid-body portion, and a proximal end
portion, the body defining a lumen extending between the distal end
portion and the proximal end portion, the body having external and
lumenal surfaces, the body having a longitudinal length sufficient
to provide fluid communication between an anterior chamber and a
tear film of the eye through the lumen when the device is implanted
in a sclera of the eye, wherein the mid-body portion defines an
opening for sclera tissue to grow through.
2. The device of claim 1, wherein a distal edge of the distal end
portion is radiused.
3. The device of claim 1, wherein a proximal edge of the proximal
end portion is radiused.
4. The device of claim 1, wherein the proximal end portion is
laterally wider than the mid-body and distal end portions.
5. The device of claim 4, wherein the mid-body portion is laterally
wider than the distal end portion.
6. The device of claim 1, wherein the mid-body portion comprises
lateral protrusions.
7. The device of claim 1, wherein an entirety of the body has a
consistent thickness.
8. The device of claim 1, wherein a distal edge of the proximal end
portion is radius to follow a curvature of the eye.
9. The device of claim 1, wherein a distal edge of the distal end
portion is semi-circular.
10. The device of claim 1, wherein the body includes a laterally
flared portion between the distal end portion and the mid-body
portion.
11. The device of claim 1, wherein the lumenal surface of the
device comprises a hydrophilic material.
12. The device of claim 11, wherein the hydrophilic material
comprises polyethylene glycol.
13. The device of claim 1, wherein the external surface of the
device is coated with a hetero-bifunctional crosslinker.
14. The device of claim 13, wherein the hetero-bifunctional
crosslinker is 5-azido-2-nitrobenzoic acid
N-hydroxysuccinimide.
15. The device of claim 1, wherein the external surface of the
device includes one or more surface areas configured to provide
increased friction with the sclera.
16. The device of claim 15, wherein the one or more surface areas
configured to provide increased friction with the sclera includes
an oxygen plasma etched surface area.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. application Ser.
No. 16/315,499 filed on Jan. 4, 2019, which is a U.S. National
Stage Application of International Application No.
PCT/US2017/040738 filed Jul. 5, 2017, which claims the benefit of
U.S. Provisional Application No. 62/359,044 filed Jul. 6, 2016. The
disclosure of the prior applications is considered part of and is
incorporated by reference in the disclosure of this
application.
BACKGROUND
1. Technical Field
[0002] This document relates to devices and methods for the
treatment of glaucoma. For example, this document provides devices
configured for implantation into the sclera of an afflicted eye to
allow aqueous humor to flow from the anterior chamber of the
afflicted eye through a lumen of the device and into the tear film,
as well as methods for using such devices to treat glaucoma. This
outflow of aqueous humor into the tear film can reduce the
intraocular pressure of an afflicted eye in addition to providing
moisture and lubrication on to the surface of the eye.
2. Background Information
[0003] Glaucoma is the leading cause of irreversible blindness in
the world. About 105 million people worldwide have glaucoma, and
nearly 10 million are bilaterally blind from this disease. In the
United States, over 3 million people suffer from glaucoma, and it
is the third most common reason for adults to visit a medical
doctor. Elevated intraocular pressure is the outstanding risk
factor for the development of glaucoma, and the main reason for
progression of the disease. Accordingly, one mode for treatment of
glaucoma is directed to lowering the intraocular pressure in the
affected eye.
[0004] Dry eye syndrome is a common condition that occurs when a
person's tears are not produced properly, or when the tears are not
of the correct consistency and evaporate too quickly. Inflammation
of the surface of the eye may occur along with dry eye. If left
untreated, this condition can lead to pain, ulcers, or scars on the
cornea, and some loss of vision.
SUMMARY
[0005] This document provides devices and methods for the treatment
of glaucoma. For example, this document provides devices configured
for implantation into the sclera of an afflicted eye to allow
aqueous humor to flow from the anterior chamber of the afflicted
eye through a lumen of the device and into the tear film, as well
as methods for using such devices to treat glaucoma. By the
strategic selection of particular materials of construction, and/or
by controlling the shape and size of the lumen, in some
embodiments, a device provided herein can be filterless, or can be
designed to include a filter. A filterless glaucoma treatment
device described herein, or a glaucoma treatment device having a
filter as described herein, can be designed to prevent bacterial
ingress and to provide a desired level of outflow resistance to
achieve a desired intraocular pressure (typically a low to normal,
or slightly above normal intraocular pressure) in glaucoma
patients. Simultaneously, moisture and lubrication is provided to
the surface of the eye to alleviate the dry eye symptoms commonly
associated with glaucoma.
[0006] Hence, this document also provides devices and methods for
the treatment of dry eye conditions. For example, this document
provides devices configured for implantation into the sclera of an
afflicted eye to allow aqueous humor to flow from the anterior
chamber of the afflicted eye through a lumen of the device and into
the tear film, as well as methods for using such devices to treat
dry eye conditions. This outflow of aqueous humor into the tear
film can provide moisture and lubrication to the surface of the
eye. The devices and methods described herein can be used for
treatment of dry eye conditions in conjunction with glaucoma
treatments, or specifically directed to dry eye alone (without
simultaneously treating glaucoma).
[0007] In one aspect, the disclosure is directed to a device for
treating glaucoma in an eye that includes a body having a distal
end portion and a proximal end portion. The body defines a lumen
extending between the distal end portion and the proximal end
portion. The body has external and lumenal surfaces. The body has a
longitudinal length sufficient to provide fluid communication
between an anterior chamber and a tear film of the eye through the
lumen when the device is implanted in a sclera of the eye. A distal
edge of the distal end portion has a radius.
[0008] Such a device for treating glaucoma in an eye may optionally
include one or more of the following features. The radius of the
distal edge may be centered on a longitudinal axis of the device.
The radius of the distal edge may extend along an arc from a first
lateral edge of the distal end portion to a second lateral edge of
the distal end portion. The radius of the distal edge may be
between 0.2 mm to 0.8 mm.
[0009] In another aspect, this disclosure is directed to a device
for treating glaucoma in an eye that includes a body having a
distal end portion and a proximal end portion. The body defines a
lumen extending along a longitudinal axis of the body between the
distal end portion and the proximal end portion. The body has
external and lumenal surfaces. The body has a longitudinal length
sufficient to provide fluid communication between an anterior
chamber and a tear film of the eye through the lumen when the
device is implanted in a sclera of the eye. The distal end portion
is laterally flared.
[0010] Such a device for treating glaucoma in an eye may optionally
include one or more of the following features. A lateral width of
the laterally flared distal end portion may increase along the
distal end portion toward the proximal end portion. A lateral width
of the laterally flared distal end portion may increase by a total
of between 0.3 mm to 1.0 mm along the distal end portion toward the
proximal end portion. The laterally flared distal end portion may
include a first lateral edge and a second lateral edge. The first
lateral edge and the second lateral edge may each be nonparallel
with the longitudinal axis. The first lateral edge and the second
lateral edge may each define angles in relation to the longitudinal
axis between 5 degrees and 30 degrees.
[0011] In another aspect, this disclosure is directed to a device
for treating glaucoma in an eye. The device includes a body having
a distal end portion, a proximal end portion, and a mid-body
portion extending between the distal end portion and the proximal
end portion. The body defines a lumen extending along a
longitudinal axis of the body between the distal end portion and
the proximal end portion. The body has external and lumenal
surfaces. The body has a longitudinal length sufficient to provide
fluid communication between an anterior chamber and a tear film of
the eye through the lumen when the device is implanted in a sclera
of the eye. The mid-body portion is laterally narrower than some
portions of each the distal end portion and the proximal end
portion.
[0012] Such a device for treating glaucoma in an eye may optionally
include one or more of the following features. A maximum total
lateral width of the mid-body portion may be at least 0.3 mm less
than a maximum total lateral width of the distal end portion. The
maximum total lateral width of the mid-body portion may be at least
0.5 mm less than a maximum total lateral width of the proximal end
portion. The mid-body portion may include a plurality of lateral
protrusions. At least some edges of the lateral protrusions may
extend laterally along angles that are non-orthogonal in relation
to the longitudinal axis.
[0013] In another aspect, this disclosure is directed to a device
for treating glaucoma in an eye. The device includes a body having
a distal end portion and a proximal end portion. The body defines a
lumen extending between the distal end portion and the proximal end
portion. The body has external and lumenal surfaces. The body has a
longitudinal length sufficient to provide fluid communication
between an anterior chamber and a tear film of the eye through the
lumen when the device is implanted in a sclera of the eye. A
proximal edge of the proximal end portion has a radius.
[0014] Such a device for treating glaucoma in an eye may optionally
include one or more of the following features. The radius of the
proximal edge may be centered on a longitudinal axis of the device.
The radius of the proximal edge may extend along an arc from a
first lateral edge of the proximal end portion to a second lateral
edge of the proximal end portion. The radius of the proximal edge
may be between 5.0 mm to 10.0 mm. The radius of the proximal edge
may be a first radius, and a distal edge of the proximal end
portion may have a second radius. The distal edge of the proximal
end portion may abut an outer surface of the eye when the device is
implanted in the sclera of the eye. The second radius may be
between 5.0 mm to 10.0 mm. The first radius may be between 5.0 mm
to 10.0 mm.
[0015] In another aspect, this disclosure is directed to a device
for treating glaucoma in an eye. The device includes a body having
a distal end portion and a proximal end portion. The body defines a
lumen extending along a longitudinal axis of the body between the
distal end portion and the proximal end portion. The body has
external and lumenal surfaces. The body has a longitudinal length
sufficient to provide fluid communication between an anterior
chamber and a tear film of the eye through the lumen when the
device is implanted in a sclera of the eye. A maximum longitudinal
length of the body in comparison to a maximum lateral width of the
body is a ratio between 1:1 to 3:1.
[0016] Any one or more of the device implementations described
above may optionally include one or more of the following features.
The proximal end portion may include at least one suture attachment
feature configured for receiving a suture to attach the body to the
eye. The lumen may be open from the first end to the second end and
configured to maintain a desired intraocular pressure without a
porous element inside the lumen. The body may include one or more
ribs extending longitudinally through at least a portion of the
lumen. The lumenal surface of the device may include a hydrophilic
material. The hydrophilic material may include polyethylene glycol.
The external surface of the device may be coated with a
hetero-bifunctional crosslinker to stimulate collagen binding. The
hetero-bifunctional crosslinker may be 5-azido-2-nitrobenzoic acid
N-hydroxysuccinimide. In some embodiments, a porous element (e.g.,
a filter material and the like) is positioned in the lumen.
[0017] In another implementation, a method for treating glaucoma
includes providing any one of the devices described herein, and
implanting the device in the sclera of the eye such that aqueous
humor flows from the anterior chamber to the tear film of the
eye.
[0018] Such a method may optionally include one or more of the
following features. After implanting the device, the second end may
protrude from the eye by a distance in the range from about 100
.mu.m to about 500 .mu.m, or from about 50 .mu.m to about 1000
.mu.m. Such protrusion can be tolerated by a patient, as with each
blink the rectus muscles retract the eyeball by about 1000 .mu.m. A
portion of the second end may be flared or otherwise extended, and
a surface of the flared or extended portion may be in contact with
the eye and generally follow a contour of the eye.
[0019] Particular embodiments of the subject matter described in
this document can be implemented to realize one or more of the
following advantages. In some embodiments, the devices provided
herein drain aqueous humor into the tear film, rather than into the
subconjuctival space. Therefore, no conjunctival bleb is formed,
and therefore there is no potential to scar. Aqueous humor can be
expelled into the tear film, thereby enhancing moisture and
lubrication to the surface of the eye. Drainage of aqueous humor
from the subject device into the tear film can alleviate dry eye
symptoms in the glaucoma patients in which it is implanted. In some
embodiments, the lumen of the devices provided herein is sized
and/or provided with a surface chemistry to resist bacteria
ingress. In addition, the geometry of the lumen can be selected to
provide a particular aqueous humor outflow resistance that yields
desirable intraocular pressure. By the selection of such a
geometry, a filterless construct is facilitated in some
embodiments. In some embodiments, a filter or filter-like element
is included in the lumen. In some embodiments, the materials used
to make a device provided herein can be selected to provide bulk
biocompatibility by seeking to match scleral rigidity, and/or by
providing a porous cellular ingrowth surface on the portion of the
device that is in contact with eye tissue. In some embodiments,
naturally occurring extracellular matrix proteins such as collagen
type 1, laminin, fibronectin, or other cell adhesion peptides
(CAPs) can be grafted onto the outer surface to promote
biointegration. In some cases, the inner or outer surfaces of the
device can be coated with materials such as polymer coatings or
biologically active molecules, to promote surface biocompatibility
and/or immobilization of the implanted device. Biointegration and
scleral rigidity matching can serve to limit inflammation by
limiting micromotion of the device. In some embodiments, suture
attachment features can be included to allow for device
stabilization before and during biointegration. In some
embodiments, a protruding portion of the devices provided herein
can be flanged or otherwise extended.
[0020] Unless otherwise defined, all technical and scientific terms
used herein have the same meaning as commonly understood by one of
ordinary skill in the art to which this invention pertains.
Although methods and materials similar or equivalent to those
described herein can be used to practice the invention, suitable
methods and materials are described herein. All publications,
patent applications, patents, and other references mentioned herein
are incorporated by reference in their entirety. In case of
conflict, the present specification, including definitions, will
control. In addition, the materials, methods, and examples are
illustrative only and not intended to be limiting.
[0021] The details of one or more embodiments of the invention are
set forth in the accompanying drawings and the description herein.
Other features, objects, and advantages of the invention will be
apparent from the description and drawings, and from the
claims.
DESCRIPTION OF THE DRAWINGS
[0022] FIG. 1 is a sagittal cross-sectional schematic diagram of an
eye with one embodiment of a device illustrative of the devices
provided herein implanted in the eye.
[0023] FIG. 2 is a perspective view of an example device for
treating glaucoma in accordance with some embodiments.
[0024] FIG. 3 is a longitudinal cross-sectional view of the device
of FIG. 2.
[0025] FIG. 4 is a schematic drawing of a sagittal cross-section of
an eye (dividing the nasal and temporal halves of the eye) that
shows example geometric relationships between the eye and an
implanted device for treating glaucoma.
[0026] FIG. 5 is a perspective view of another example device for
treating glaucoma in accordance with some embodiments.
[0027] FIG. 6 is a perspective view of another example device for
treating glaucoma in accordance with some embodiments.
[0028] FIG. 7 is a side view of the device of FIG. 6.
[0029] FIG. 8 is a sagittal cross-sectional schematic diagram of an
eye with the device of FIG. 6 implanted in the eye.
[0030] FIG. 9 is a perspective view of another example device for
treating glaucoma in accordance with some embodiments.
[0031] FIG. 10 is a side view of the device of FIG. 9.
[0032] FIG. 11 is a perspective view of another example device for
treating glaucoma in accordance with some embodiments.
[0033] FIG. 12 is a side view of the device of FIG. 11.
[0034] FIG. 13 is a perspective view of another example device for
treating glaucoma in accordance with some embodiments.
[0035] FIG. 14 is a side view of the device of FIG. 13.
[0036] FIG. 15 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. An enlarged
view of a portion of the lumenal structure is illustrated.
[0037] FIG. 16 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. An enlarged
view of a portion of the lumenal structure is illustrated.
[0038] FIG. 17 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. An enlarged
view of a portion of the lumenal structure is illustrated.
[0039] FIG. 18 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. An enlarged
view of a portion of the lumenal structure is illustrated.
[0040] FIG. 19 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. An enlarged
view of a portion of the lumenal structure is illustrated.
[0041] FIG. 20 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. An enlarged
view of a portion of the lumenal structure is illustrated.
[0042] FIG. 21 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. An enlarged
view of a portion of the lumenal structure is illustrated.
[0043] FIG. 22 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. An enlarged
view of a portion of the lumenal structure is illustrated.
[0044] FIG. 23 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. An enlarged
view of a portion of the lumenal structure is illustrated.
[0045] FIG. 24 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. An enlarged
view of a portion of the lumenal structure is illustrated.
[0046] FIG. 25 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. An enlarged
view of a portion of the lumenal structure is illustrated.
[0047] FIG. 26 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. An enlarged
view of a portion of the lumenal structure is illustrated.
[0048] FIG. 27 is an exploded perspective view of another example
device for treating glaucoma in accordance with some
embodiments.
[0049] FIG. 28 is a side view of the device of FIG. 27.
[0050] FIG. 29 is an exploded perspective view of another example
device for treating glaucoma in accordance with some
embodiments.
[0051] FIG. 30 is a side view of the device of FIG. 29.
[0052] FIG. 31 is a sagittal cross-sectional schematic diagram of
an eye with another embodiment of a device illustrative of the
devices provided herein implanted in the eye.
[0053] FIG. 32 is a perspective view of another example device for
treating glaucoma in accordance with some embodiments.
[0054] FIG. 33 is a perspective view of another example device for
treating glaucoma in accordance with some embodiments.
[0055] FIG. 34 is a photograph of an example eye shortly after
receiving an implantation of two devices in accordance with some
embodiments.
[0056] FIG. 35 is a photograph of the eye of FIG. 34 two weeks
after the implantation.
[0057] FIG. 36 is a photograph of the eye of FIG. 34 one month
after the implantation.
[0058] FIG. 37 is an exploded perspective view of another example
device for treating glaucoma in accordance with some
embodiments.
[0059] FIG. 38 is a side view of the device of FIG. 37.
[0060] FIG. 39 is a sagittal cross-sectional schematic diagram of
an eye with the device of FIG. 37 implanted in the eye.
[0061] FIG. 40 is an exploded plan view of an example deployment
tool and a device for treating glaucoma.
[0062] FIG. 41 is an exploded side view of the example deployment
tool and the device for treating glaucoma of FIG. 40.
[0063] FIG. 42 is a plan view of another example device for
treating glaucoma in accordance with some embodiments.
[0064] FIG. 43 is a lateral side elevation view of the device of
FIG. 42.
[0065] FIG. 44 is a plan view of another example device for
treating glaucoma in accordance with some embodiments.
[0066] FIG. 45 is a lateral side elevation view of the device of
FIG. 44.
[0067] FIG. 46 is a plan view of another example device for
treating glaucoma in accordance with some embodiments.
[0068] FIG. 47 is a lateral side elevation view of the device of
FIG. 46.
[0069] FIG. 48 is a plan view of another example device for
treating glaucoma in accordance with some embodiments.
[0070] FIG. 49 is a lateral side elevation view of the device of
FIG. 48.
[0071] FIG. 50 is a plan view of another example device for
treating glaucoma in accordance with some embodiments. The device
is shown in a first configuration.
[0072] FIG. 51 is a plan view of the device of FIG. 50 in a second
configuration.
[0073] FIG. 52 is a plan view of an example insertion tool.
[0074] FIG. 53 is a side view of the insertion tool of FIG. 52.
[0075] Like reference numbers represent corresponding parts
throughout.
DETAILED DESCRIPTION
[0076] This document provides devices and methods for the treatment
of glaucoma and/or dry eye conditions. For example, this document
provides devices configured for implantation into the sclera of an
afflicted eye to allow aqueous humor to flow from the anterior
chamber of the afflicted eye through a lumen of the device and into
the tear film, as well as methods for using such devices to treat
glaucoma and/or dry eye. By the strategic selection of particular
materials of construction, and/or by controlling the shape and size
of the lumen, in some embodiments, a device provided herein can be
filterless, or can be designed to include a filter. A filterless
glaucoma treatment device described herein, or a glaucoma treatment
device having a filter as described herein, can be designed to
prevent bacterial ingress and to provide a desired level of outflow
resistance to achieve a desired intraocular pressure (typically a
low to normal, or slightly above normal intraocular pressure) in
glaucoma patients. The flow of aqueous humor from the anterior
chamber also provides moisture and lubrication to the surface of
the eye to alleviate the dry eye symptoms commonly associated with
the use of eye drops for treating glaucoma.
[0077] Referring to FIG. 1, an example device 1 is shown implanted
in an afflicted eye 20 for the purpose of treating glaucoma and/or
dry eye of afflicted eye 20. The depicted anatomical features of
eye 20 include an anterior chamber 2, a sclera 6, a tear film 4, an
iris 23, a ciliary body 25, and a cornea 21. Device 1 includes a
body 3 that defines a lumen 5. Body 3 includes a first end 7 and a
second end 9. Body 3 has an external surface 10, and a lumenal
surface 12.
[0078] As depicted, device 1 is configured such that, according to
some implementations, device 1 can be surgically implanted in
sclera 6 of eye 20. Device 1 has a length sufficient to provide
fluid communication between anterior chamber 2 and tear film 4 of
eye 20 when device 1 is implanted in sclera 6. As described further
herein, in some embodiments, lumen 5 can be sized and configured to
provide an appropriate outflow resistance to modulate aqueous humor
flowing through lumen 5, without an element that provides
additional flow resistance (e.g., a filter or a porous element). In
doing so, lumen 5 functions to maintain a desired intraocular
pressure (TOP) to treat a glaucoma-afflicted eye 20, while also
providing moisture and lubrication to the surface of eye 20 and
tear film 4. In other words, aqueous humor is shunted directly to
tear film 4. According to some implementations, no conjunctival
bleb is formed. Additionally, no episcleral venous pressure (EVP)
is created that could raise nocturnal TOP. EVP is unaffected by the
use of the devices and methods provided herein. In some cases, a
device provided herein can define a lumen that includes a filter or
a porous element.
[0079] In some cases, to provide fluid communication between
anterior chamber 2 and tear film 4, device 1 has a length of about
2.5 mm. In some embodiments, device 1 has a length of between about
2.5 mm and about 5.0 mm, or between about 3.5 mm and about 6.0 mm.
The length of at least about 2.5 mm will reduce the possibility of
blockage of the lumenal opening in anterior chamber 2 by iris 23.
The length of device 1 within the scleral tract would preferably be
greater than the scleral thickness, because insertion would not be
perpendicular to sclera 6 (but more tangential) to be parallel to
iris 23.
[0080] In some cases, device 1 is designed such that the modulus of
elasticity of device 1 is essentially equal to the modulus of
elasticity of sclera 6. Such a matching of the moduli of elasticity
of device 1 to sclera 6 is advantageous for at least the following
reasons. When an implant is placed in the body, for best results
the implant should handle local mechanical loads in a same or very
similar way as the surrounding tissue. If the modulus of elasticity
of the implant is significantly higher than the surrounding tissue,
it will take over the load bearing and the surrounding tissue will
start to die. This causes the implant to loosen, and eventually
fall out. Alternatively, when the modulus of elasticity of the
implant is significantly lower than the tissue, it can cause excess
load on the tissue, again leading to a loose implant which may
eventually fall out. The best approach in designing a biomaterial
is to match the surrounding tissue's modulus of elasticity. The
surrounding tissue will experience stress loading in much the same
way it did before the implant, leading to good healing, with
significantly reduced micromotion when compared to the same implant
with a mismatched modulus. Such matching of the moduli of
elasticity of device 1 to sclera 6 can be achieved through material
selection and/or the mechanical design of device 1.
[0081] Referring also to FIGS. 2 and 3, additional details and
features of example device 1 are visible therein. FIG. 3 is a
longitudinal cross-sectional view of device 1 along section line
3-3 as shown in FIG. 2. It should be understood that one or more
(or all) of the details and features described herein in reference
to example device 1 are also applicable to the other device
embodiments provided herein.
[0082] In some embodiments, the main structure of body 3 is formed
of a material such as, but not limited to, SU-8, parylene,
thiolene, silicone, acrylic, polyimide, polypropylene, polymethyl
methacrylate, polyethylene terephthalate (PET), polyethylene glycol
(PEG), thermoplastic polyurethane (TPU), polyurethane, and expanded
polytetrafluoroethylene (e.g., denucleated and coated with
laminin). In some embodiments, the main structure of body 3 is
formed of a combination of two or more materials. For example, in
some embodiments, a layer of PEG is sandwiched between an upper
layer of PET and a lower layer of PET. The PEG can be used to
define lumen 5, in some embodiments. The use of PEG for the
surfaces of the lumen can be advantageous because PEG resists
bacterial, protein, and cell adherence. In some embodiments,
materials that prevent or resist bio-fouling can be incorporated
into device 1 (and the other devices described herein). For
example, in some embodiments triethylene glycol, Poly(ethylene)
glycol, zwitterionic polymers (e.g. poly(carboxybetaine
methacrylate)), poly(2-oxaline)s (e.g. poly(2-ethyl-2-oxaline)),
poly(hydroxyfunctional acrylates) (e.g. poly(2-hydroxyethyl
methacrylate)), poly(vinylpyrrolidone), peptides or peptoids (e.g.
poly(amino acid) or poly(petoid)) can be incorporated into one or
more portions of, or an entirety of, device 1.
[0083] In some embodiments, a portion of external surface 10 of
body 3 is coated with a coating such as a silicone coating or other
type of coating. In some embodiments, substantially the entire
external surface 10 is coated with a coating such as a silicone
coating or other type of coating. In particular embodiments, one
portion of external surface 10 may be coated with silicone, and
other one or more portions may be coated with another type or types
of coatings. Embodiments that include a silicone coating on
portions or all of external surface 10 may be coated with a layer
of silicone about 50 .mu.m thick, or within a range from about 40
.mu.m to about 60 .mu.m thick, or within a range from about 30
.mu.m to about 70 .mu.m thick, or within a range from about 20
.mu.m to about 80 .mu.m thick, or thicker than about 80 .mu.m.
[0084] In some embodiments, external surface 10 of body 3 includes
a porous cellular ingrowth coating on at least a portion thereof.
In some embodiments, the portion of external surface 10 that is
coated with the cellular ingrowth coating corresponds substantially
to the portion of body 3 in contact with eye tissue (e.g., sclera
6) following scleral implantation. Such porous cellular ingrowth
coatings have been described with respect to other ophthalmic
implants, and can be made of silicone with a thickness of about
0.04 mm, in some examples. In some embodiments, surface laser
engraving can be used to make depressions in a portion of the body
surface to allow cellular ingrowth. Selected growth factors may be
adsorbed on to this coating to enhance cellular ingrowth. Coating
external surface 10 with a hetero-bifunctional crosslinker allows
the grafting of naturally occurring extracellular matrix proteins
such as collagen type 1, laminin, fibronectin, or other cell
adhesion peptides (CAPS) to external surface 10. These can attract
fibroblasts from the episclera to lead to collagen immobilization
of device 1. One example of a hetero-bifunctional crosslinker that
is useful for such a purpose is 5-azido-2-nitrobenzoic acid
N-hydroxysuccinimide.
[0085] In some embodiments, one or more portions of body 3 may be
configured to inhibit conjunctival overgrowth. For example, second
end 9 (of which at least a portion thereof extends exterior to
cornea 21) can be configured to inhibit conjunctival overgrowth.
Preventing such conjunctival overgrowth can advantageously
facilitate patency of lumen 5. In some such embodiments, a coating
such as a PEG coating can be applied to second end 9 to inhibit
conjunctival overgrowth.
[0086] In some embodiments, a bio-inert polymer is included as a
liner of lumen 5. That is, in some embodiments, lumenal surface 12
includes a bio-inert polymer material. For example, in some
embodiments, a material such as, but not limited to, polyethylene
glycol (PEG), phosphoryl choline (PC), or polyethylene oxide (PEO)
can be used for the lumenal surface 12 of lumen 5. Such bio-inert
surfaces may be further modified with biologically active molecules
such as heparin, spermine, surfactants, proteases, or other
enzymes, or other biocompatible chemicals amendable to surface
immobilization or embedding. Some such materials are advantageously
hydrophilic. For example, in some embodiments, the hydrophilic
properties of lumenal surface 12 can help prevent bacterial
contamination of device 1.
[0087] In some embodiments, a filter or filter-like porous member
is included in the device's flow path (e.g., lumen 5) for the
aqueous humor. In some embodiments, no filter or porous member is
present in lumen 5 for the purpose of resisting ingress of
bacteria. In some cases, the surface chemistry of lumen 5 of a
device provided herein can be used to prevent bacterial ingress.
For example, the high molecular weight PEG lining lumen 5 can be
very hydrophilic and can attract a hydration shell. The motility of
the PEG side chains, and steric stabilization involving these side
chains, also can repulse bacteria, cells, and proteins. In some
cases, the shear stress of the laminar flow of the aqueous humor as
it leaves eye 20 can resist ingress of bacteria into device 1.
Experiments demonstrated that when perfusing device 1 into an
external broth with 10.sup.8 bacteria per mL, no bacteria entered
device 1. Tears are usually quite sterile and have IgA, lysozyme,
lactoferrin, and IgG/complement if inflamed. In some cases, tears
can be used to clear an infection.
[0088] In some embodiments, device 1 is constructed using bulk and
surface micro-machining. In some embodiments, device 1 is
constructed using 3D micro-printing. In particular embodiments,
external surface 10 is textured such as by stippling,
cross-hatching, waffling, roughening, plasma etching, photo
etching, chemical etching, placing backwards facing barbs or
protrusions, and the like. One way to accomplish this external
surface texturing is by laser engraving. Such featuring can
stabilize device 1 in situ and also can increase the visibility of
device 1 by making it less transparent. The featuring of the
external surface 10 can make device 1 more visible to a surgeon,
thereby making the handling and deployment process of device 1 more
efficient and convenient.
[0089] In some embodiments, the width W of device 1 is in a range
from about 0.1 mm to about 0.4 mm, or from about 0.3 mm to about
0.6 mm, or from about 0.5 mm to about 0.8 mm, or from about 0.7 mm
to about 1.0 mm, or from about 0.9 mm to about 1.2 mm, or from
about 1.1 mm to about 1.4 mm, or from about 1.3 mm to about 1.6 mm,
or from about 1.5 mm to about 1.8 mm, or greater than about 1.8
mm.
[0090] In the depicted embodiment, body 3 flares and/or extends out
around at least part of second end 9. The flaring of body 3 at its
second end 9 provides a number of advantages. For example, flaring
of body 3 at its second end 9 aids in the surface mounting of
device 1 in eye 20 by providing an endpoint of insertion as device
1 is pushed into sclera 6 during surgery. Additionally, the flaring
of body 3 at its second end 9 provides structural support to
bolster the portion of device 1 that protrudes from eye 20. Such
structural support can help maintain patency of lumen 5 by
resisting deflection of the protruding portion, which may tend to
occur from the forces exerted by an eyelid, for example. For
instance, such a posteriorly placed flare/extension bolsters the
device against posterior pressures. In some cases, the
flaring/extending of body 3 at its second end 9 provides additional
resistance to growth of conjunctiva over the exposed second end 9.
For example, the additional surface area provided by the flared
portion may tend to make growth of conjunctiva over the exposed
second end 9 less likely to occur, thereby helping to maintain
patency of lumen 5.
[0091] In some cases, device 1 can be anteriorly beveled at its
first end 7 to assist in implantation and to keep the iris from
plugging the inner lumenal opening.
[0092] In the depicted embodiment, lumen 5 is a narrow slit with a
generally rectangular cross-section. This narrow slit may contain a
number of longitudinal channels, which themselves may be square,
rectangular, circular, or the like, and combinations thereof. In
some embodiments, the total width of lumen 5 is about 0.5 mm. In
some embodiments, the total width of lumen 5 is in a range from
about 0.4 mm to about 0.6 mm, or about 0.3 mm to about 0.7 mm, or
about 0.2 mm to about 0.8 mm. The height, effective width,
configuration, and length of lumen 5 can be selected to provide a
total resistance so that a desirably low TOP from about 8 mm Hg to
about 12 mm Hg is maintained. This TOP is sometimes called the
threshold pressure, which is the TOP at which pressure does not
contribute to loss of retinal ganglion cells over and above the
normal age-related loss. The devices provided herein for providing
glaucoma and/or dry eye treatment can be configured to attain the
threshold pressure, without inducing hypotony.
[0093] The effective width of lumen 5 is that width obtained after
subtracting the total width of all the device support ribs 13 (as
shown in FIG. 2). In some implementations, it is desirable to
achieve a normal aqueous humor outflow resistance of about 3.2
mmHg.times.min/.mu.L. In some implementations, there is some
tolerance in the system, since the aqueous humor outflow even in a
glaucomatous eye is rarely zero. In fact, the main natural aqueous
humor outflow of the eye, the conventional or trabecular meshwork
pathway, is TOP dependent and can modify TOP swings. Poiseuille's
equation for laminar flow though a porous media
(R=8.times.viscosity.times.channel length/channel
number.times..pi..times.channel radius to the fourth power) can be
used to determine the combination of lumen dimensions to give the
proper resistance to provide the desired TOP.
[0094] In the depicted embodiment, device 1 includes a suture
attachment feature 11. In the depicted embodiment, suture
attachment feature 11 is a through-hole that extends completely
through body 3. Suture attachment feature 11 can receive a suture
therethrough, whereby body 3 is attached to eye 20. In some
implementations, such suture(s) can stabilize device 1 in eye 20
prior to bio-integration of device 1 with eye 20. In some
embodiments, one or more other types of suture attachment features
are included such as a flange, a slot, a projection, a clamp, and
the like. In the depicted embodiment, suture attachment feature 11
is a rectangular hole. In some embodiments, suture attachment
feature 11 is a circular hole, ovular hole, or another shape of
hole.
[0095] In some embodiments, suture attachment feature 11 is sized
large enough to receive a 10-0 spatula needle. For example, in some
embodiments, the dimensions of suture attachment feature 11 is
about 300 .mu.m by about 200 .mu.m. Other appropriate sizes for
suture attachment feature 11 can be used.
[0096] In some embodiments, one or more longitudinal support ribs
13 is included within lumen 5. Support rib 13 can add structural
rigidity to help maintain patency of lumen 5. In some embodiments,
support rib 13 includes a series of short discontinuous ribs that
are disposed along lumen 5. In some embodiments, no support rib 13
is included.
[0097] In some embodiments, longitudinal support ribs 13 can divide
lumen 5 into two or more portions (e.g., channels). That is, in
some embodiments, lumen 5 of body 3 includes two or more channels
(e.g., two, three, four, five, six, or more than six channels).
Aqueous outflow can occur through these channels, which may be
square, rectangular, circular, and the like, and combinations
thereof.
[0098] In some embodiments, the portion of body 3 that is in
contact with eye tissue following implantation includes one or more
barbs designed to engage with tissue upon implantation and provide
stability to implanted device 1. The one or more barbs may be
formed as part of device body 3 during manufacture, or may be fused
or bonded to device body 3 using any appropriate technique.
[0099] It should be understood that one or more (or all) of the
details and features described herein in reference to example
device 1 are also applicable to the other device embodiments
provided herein. Moreover, one or more of the device details and
features described herein can be combined with one or more other
device details and features described herein to create hybrid
device constructions, and such hybrid device constructions are
within the scope of this disclosure.
[0100] Referring also to FIG. 4, certain geometric aspects of
device 1 in relation to eye 20 can be described. Device 1 is shown
implanted at the limbus of eye 20 in accordance with some example
implant techniques. The dimension X is the anterior protrusion of
device 1 from the scleral surface, and the dimension Y is the
posterior protrusion of device 1 from the scleral surface. In the
depicted implementation, dimensions X and Y are about the same
because flare bevel angle Z follows the contour of eye 20 (e.g.,
angle .theta. is about 40.degree. to 45.degree. in the depicted
implementation). The posterior flare and/or extension also follows
the contour of eye 20. Protrusion of device 1 from the scleral
surface can prevent conjunctival overgrowth. In some cases, this
advantage should be balanced with the fact that increased
protrusion may tend to make for increased micromotion in some
cases. In some embodiments, protrusion dimensions X and Y are in a
range from about 50 .mu.m to about 1000 .mu.m, or from about 50
.mu.m to about 200 .mu.m, or from about 100 .mu.m to about 300
.mu.m, or from about 200 .mu.m to about 400 .mu.m, or from about
300 .mu.m to about 500 .mu.m, or from about 400 .mu.m to about 600
.mu.m, or from about 500 .mu.m to about 700 .mu.m, or from about
600 .mu.m to about 800 .mu.m, or from about 700 .mu.m to about 900
.mu.m, or from about 800 .mu.m to about 1,000 .mu.m.
[0101] Dimension A in FIG. 4 is the thickness of device 1.
Dimension B is the frontal view thickness of the flared portion of
device 1. In some embodiments, facial dimensions A and B are about
200 .mu.m. Dimension B can vary in correspondence to variations in
selected protrusion dimensions X and Y.
[0102] In some cases, device 1 is implanted in eye 20 at a position
that is at about 12 o'clock relative to eye 20 (when viewed from
the front of the eye). In other words, in some cases, device 1 is
implanted at the limbus of eye 20 in the most superior position
possible. In other cases, device 1 is implanted at the limbus of
eye 20 at a position that is at least somewhat lateral from the
most superior 12 o'clock position. For example, when viewed from
the front of the eye, device 1 can be implanted between the 9
o'clock and 11 o'clock positions, or between the 10 o'clock and 12
o'clock positions, or between the 11 o'clock and 1 o'clock
positions, or between the 12 o'clock and 2 o'clock positions, or
between the 1 o'clock and 3 o'clock positions, or between the 10
o'clock and 2 o'clock positions, or between the 9 o'clock and 3
o'clock positions.
[0103] As an alternative to implantation of device 1 via the limbus
of eye 20, in some cases device 1 can be implanted farther away
from the cornea of eye 20. For example, in some cases device 1 can
be implanted under the subconjunctiva. To implant device 1 under
the subconjunctiva, a subconjunctiva bleb would be created in which
the protruding portion of device 1 would reside. Such a bleb would
be located under an eyelid such as the upper eyelid of the lower
eyelid. For example, in some cases device 1 is implanted under the
subconjunctiva of eye 20 at a position that is at about 12 o'clock
relative to eye 20 (when viewed from the front of the eye). In some
cases, when viewed from the front of the eye, device 1 can be
implanted under the subconjunctiva of eye 20 between the 9 o'clock
and 11 o'clock positions, or between the 10 o'clock and 12 o'clock
positions, or between the 11 o'clock and 1 o'clock positions, or
between the 12 o'clock and 2 o'clock positions, or between the 1
o'clock and 3 o'clock positions, or between the 10 o'clock and 2
o'clock positions, or between the 9 o'clock and 3 o'clock
positions.
[0104] Referring to FIG. 5, another example device 100 in
accordance with some embodiments provided herein is illustrated.
Device 100 includes a body 103 that defines a lumen 105. Body 103
includes a first end 107 and a second end 109. Body 103 has an
external surface 110 and a lumenal surface 120.
[0105] Device 100 can be constructed using any of the materials and
techniques as described above in reference to device 1. In some
cases, device 100 can be configured and used as described above in
reference to device 1. Device 100 differs from device 1, at least
in regard to, the addition of lateral wings 110a and 110b. Further,
in the depicted embodiment of device 100, device 100 does not
include suture attachment feature 11 as included in device 1.
Rather, device 100 includes suture attachment features 111a and
111b that are disposed in wings 110a and 110b, respectively. Each
of suture attachment features 111a and 111b can be configured like
suture attachment feature 11 of device 1 as described above.
[0106] A first method for installing the devices provided herein is
as follows. Sometime before installation, the eye is irrigated with
1-5% Betadine solution, and topical antibiotic and non-steroidal
anti-inflammatory drops (NSAID) are applied to the operative eye.
These can be continued for about one week postoperatively four
times a day. The NSAID helps stabilize the blood-aqueous
barrier.
[0107] Each of the embodiments of the device illustrated herein may
be inserted under topical anesthesia, possibly supplemented
subconjunctivally. In general, the devices provided herein may be
inserted into the sclera and under the conjunctiva, using an
operative procedure. The location of insertion of a device provided
herein can be in the sclera at about the posterior surgical limbus.
In some cases, a device provided herein can be inserted at any site
around the limbus. In some cases, a device provided herein can be
inserted at the superior or temporal limbus. In some cases, a
device provided herein can be inserted under the subconjunctiva
such that the protruding portion of the device resides within a
bleb created in the subconjunctiva.
[0108] In some cases, the insertion procedure can begin by excising
a small amount of conjunctiva at the site of the anticipated
insertion, exposing the underlying sclera. In some cases (as
described further below), the insertion procedure is performed
without the excision of conjunctiva. Any bleeding can then be
cauterized. For embodiments of the device as shown in FIG. 5, a
groove incision can be made at the site of insertion with a diamond
blade with a depth guard to a depth sufficient to cover the entire
length of wings 110a and 110b when the device is in place. Wings
110a and 110b can provide an end-stop for insertion, so the flare
at end 109 of device 100 is optional. This groove incision can be
made at or near the posterior surgical limbus and can be parallel
to the iris plane. For the embodiment of device 1 of FIG. 2, no
groove incision is needed, since this is only necessitated by wings
110a and 110b. In some cases, for device 1, only a straight stab
incision is used, with the end-stop for insertion depth provided by
the flare/extension at the outer end of the device. In some cases,
for device 1, insertion can be made through intact conjunctiva.
[0109] Approximately 1-2 mm posterior to the limbus, at the site of
the now exposed sclera, a diamond blade can be used to make a stab
incision into the anterior chamber, while held roughly parallel to
the iris. This blade is of a size predetermined to make an opening
into the anterior chamber sized appropriately for the introduction
of the device. This stab incision is made gently, but relatively
quickly, assiduously avoiding any and all intraocular structures.
Such an uneventful paracentesis has been found not to disrupt the
blood-aqueous barrier in most cases. In any event, any disruption
of this barrier is usually of less than 24 hours duration without
continued insult.
[0110] The device is next picked up and held with a non-toothed
forceps. The lips of the stab incision wound may be gaped with a
fine, toothed forceps. The pointed tip of the tube element would
then be gently pushed through the scleral tract of the stab
incision and into the anterior chamber, with the device lying above
and parallel to the iris, with the bevel up (i.e., anteriorly). The
flare/extension in the embodiments of device 1 and device 100
provide for a definite endpoint to the depth of insertion. For
embodiments of the device having a beveled first end, the bevel is
oriented anteriorly to minimize the potential for blockage of the
lumenal opening by the iris. The scleral barb(s) or other outer
surface features (if included) stabilize the device until the
biointegration with the sclera is complete. This biointegration is
a function of its porous cellular ingrowth surface, possibly
enhanced by adsorbed growth factors and/or grafted extracellular
matrix proteins. In addition, in some implementations, one or more
sutures may be added using the device's suture attachment features
to stabilize the device prior to biointegration. For example, in
the embodiments of device 1 and device 100, a 10-0 nylon suture on
a broad spatula needle may be used to suture the device the sclera,
providing additional stability to the device until the
biointegration is complete. This suture may then be easily removed
at a later time if needed. An alternative insertion technique would
have the device pre-loaded into an insertion holder or cartridge,
to limit the needed handling of the device by the surgeon. A
properly sized sharp blade could be at the leading edge of the
inserter, such blade acting also as a guide for implanting the
device. Alternatively, the paracentesis could be made with a
separate blade, followed by controlled insertion with an
inserter.
[0111] After insertion of the device, an ocular shield can be
placed over the eye. The implanted device will bio-integrate with
the sclera, thereby reducing the risks of infections such as tunnel
infection.
[0112] Referring to FIGS. 6 and 7, another example device 600 in
accordance with some embodiments provided herein is illustrated.
Device 600 includes a body 603 that defines a lumen 605. Body 603
includes a first end 607 and a second end 609. Body 603 has an
external surface 610 and a lumenal surface 612.
[0113] Device 600 can be constructed using any of the materials and
techniques as described herein in reference to device 1. Also,
device 600 can be configured and used in any of the manners
described herein in reference to device 1.
[0114] In the depicted embodiment, first end 607 is generally
orthogonal in relation to the longitudinal surfaces of external
surface 610. In contrast, second end 609 of the depicted embodiment
is beveled in relation to the longitudinal surfaces of external
surface 610. It should be understood that, in some embodiments of
device 600 and the other devices provided herein, both ends 607 and
609 may be beveled (e.g., like second end 609), both ends 607 and
609 may be orthogonal (e.g., like first end 607), or either one of
ends 607 or 609 may be beveled while the other one of ends 607 or
609 is orthogonal.
[0115] In the depicted embodiment, lumen 605 includes a first
longitudinal rib 613a and a second longitudinal rib 613b. While in
the depicted embodiment, the ribs 613a and 613b extend continuously
from first end 607 to second end 609, in some embodiments, ribs
613a and 613b may be made of multiple individually shorter segments
and/or other arrangements. It should be understood that lumen 605
may be configured with any of the lumenal constructs provided
herein (e.g., FIGS. 15-26, and others), and combinations
thereof.
[0116] In the depicted embodiment, second end 609 includes a first
flange portion 614a and a second flange portion 614b that extend
laterally in relation to the longitudinal axis of body 603. In some
implementations, surfaces of flange portions 614a and 614b contact
the surface of the cornea and provide mechanical stabilization of
device 600 in relation to the eye. The outermost lateral surfaces
of flange portions 614a and 614b are radiused (contoured) in the
depicted embodiment. In some embodiments, the outermost lateral
surfaces of flange portions 614a and 614b are planar and parallel
to the longitudinal surfaces of external surface 610. In some
embodiments, the outer lateral surfaces of flange portions 614a and
614b are planar and unparallel or askew in relation to the
longitudinal surfaces of external surface 610.
[0117] In some embodiments, one or more suture attachment features
are included on device 600 (and the other devices provided herein).
In the depicted embodiment, second end 609 includes a first suture
attachment structure 616a and a second suture attachment structure
616b. The suture attachment structures 616a and 616b are slots in
the depicted embodiment. In some embodiments, other types of suture
attachment structures can be alternatively or additionally
included. While the depicted embodiment includes two suture
attachment structures 616a and 616b, in some embodiments, zero,
one, three, four, or more than four suture attachment structures
are included.
[0118] One or more portions of external surface 610 can be
configured for enhanced friction with eye tissue (e.g., the cornea
or sclera). Advantageous mechanical stability and/or migration
resistance of the device 600 (and the other devices provided
herein) in relation to the eye can be facilitated by such portions.
For example, in the depicted embodiment, a surface portion 618
includes an enhanced texture (roughness) in comparison to other
portions of external surface 610. In the depicted embodiment,
surface portion 618 is a waffled surface (cross-hatched). In some
embodiments, other types of texturing configurations can be
alternatively or additionally included. For example, such texturing
configurations can include, but are not limited to, stippling,
knurling, inclusion of one or more barbs, and the like, and
combinations thereof. In some embodiments, the surface portion 618
is created by techniques such as, but not limited to, laser
machining, chemical etching, 3D printing, photo etching, plasma
etching, and the like.
[0119] Referring to FIG. 8, device 600 is shown implanted in
afflicted eye 20 for the purpose of treating glaucoma and/or dry
eye of afflicted eye 20. The depicted anatomical features of eye 20
include anterior chamber 2, sclera 6, tear film 4, iris 23, ciliary
body 25, and cornea 21. Device 600 includes body 603 that defines
lumen 605. Body 603 includes first end 607 and a second end 609.
Body 603 has an external surface 610, and a lumenal surface
612.
[0120] As depicted, device 600 (and the other devices provided
herein) is configured to be surgically implanted in sclera 6 of eye
20. Device 600 has a length sufficient to provide fluid
communication between anterior chamber 2 and tear film 4 of eye 20
when device 600 is implanted in sclera 6. As described further
below, in some embodiments lumen 605 is sized and configured to
provide an appropriate outflow resistance to modulate aqueous humor
flowing through lumen 605, without the need for an element that
provides additional flow resistance (e.g., a filter or a porous
element). In doing so, lumen 605 functions to maintain a desired
TOP to treat a glaucoma afflicted eye 20, while also providing
moisture and lubrication to the surface of eye 20 and tear film 4.
In some embodiments, a filter or filter-like porous element is
includes in lumen 605.
[0121] In general, to provide fluid communication between anterior
chamber 2 and tear film 4, in some embodiments, device 600 has a
length of about 2.5 mm. In some embodiments, device 600 has a
length of from about 2.5 mm to about 5.0 mm, or from about 3.5 mm
to about 6.0 mm. The length of at least about 2.5 mm will reduce
the possibility of blockage of the lumenal opening in anterior
chamber 2 by iris 23. The length of device 600 within the scleral
tract would preferably be greater than the scleral thickness,
because insertion would not be perpendicular to sclera 6 (but more
tangential) to be parallel to iris 23.
[0122] Referring to FIGS. 9 and 10, another example device 700 in
accordance with some embodiments provided herein is illustrated.
Device 700 includes a body 703 that defines a lumen 705. Body 703
includes a first end 707 and a second end 709. Body 703 has an
external surface 710 and a lumenal surface 712.
[0123] Device 700 can be constructed using any of the materials and
techniques as described herein in reference to device 1. Also,
device 700 can be configured and used in any of the manners
described herein in reference to device 1.
[0124] In the depicted embodiment, first end 707 is beveled in
relation to the longitudinal surfaces of external surface 710.
Second end 709 of the depicted embodiment is also beveled in
relation to the longitudinal surfaces of external surface 710. It
should be understood that, in some embodiments of device 700 (and
the other devices provided herein), both ends 707 and 709 may be
beveled (e.g., as shown), both ends 707 and 709 may be orthogonal,
or either one of ends 707 or 709 may be beveled while the other one
of ends 707 or 709 is orthogonal.
[0125] In the depicted embodiment, lumen 705 includes a plurality
of ovular pillars 713 that are spaced apart from each other. It
should be understood that lumen 705 may be configured with any of
the lumenal constructs provided herein (e.g., FIGS. 15-26, and
others), and combinations thereof.
[0126] In the depicted embodiment, second end 709 includes a first
flange portion 714a and a second flange portion 714b. In some
implementations, flange portions 714a and 714b contact the surface
of the cornea and provide mechanical stabilization of device 700 in
relation to the eye. The outer lateral surfaces of flange portions
714a and 714b include planar and chamfered portions in the depicted
embodiment. In some embodiments, the outer lateral surfaces of
flange portions 714a and 714b are radiused (contoured) in relation
to the longitudinal surfaces of external surface 710.
[0127] In some embodiments, one or more suture attachment features
are included on device 700 (and the other devices provided herein).
In the depicted embodiment, second end 709 includes a suture
attachment structure 716. The suture attachment structure 716 is a
slot in the depicted embodiment. In some embodiments, other types
of suture attachment structures can be alternatively or
additionally included. While the depicted embodiment includes one
suture attachment structure 716, in some embodiments, zero, two,
three, four, or more than four suture attachment structures are
included.
[0128] One or more portions of external surface 710 can be
configured for enhanced friction with eye tissue (e.g., the cornea
or sclera). Such portions can provide advantageous mechanical
stability and/or migration resistance of the device 700 (and the
other devices provided herein) in relation to the eye. For example,
in the depicted embodiment, a surface portion 718 includes an
enhanced texture (roughness) in comparison to other portions of
external surface 710. In the depicted embodiment, surface portion
718 is a stippled surface. In some embodiments, other types of
texturing configurations can be alternatively or additionally
included. For example, such texturing configurations can include,
but are not limited to, cross-hatching, knurling, inclusion of one
or more barbs, and the like, and combinations thereof. In some
embodiments, the surface portion 718 is created by techniques such
as, but not limited to, laser machining, chemical etching, 3D
printing, plasma etching, photo etching, and the like.
[0129] Referring to FIGS. 11 and 12, another example device 800 in
accordance with some embodiments provided herein is illustrated.
Device 800 includes a body 803 that defines a lumen 805. Body 803
includes a first end 807 and a second end 809. Body 803 has an
external surface 810 and a lumenal surface 812.
[0130] Device 800 can be constructed using any of the materials and
techniques as described herein in reference to device 1. Also,
device 800 can be configured and used in any of the manners
described herein in reference to device 1.
[0131] In the depicted embodiment, first end 807 is beveled. Second
end 809 of the depicted embodiment is also beveled in relation to
the longitudinal surfaces of external surface 810. It should be
understood that, in some embodiments of device 800 and the other
devices provided herein, both ends 807 and 809 may be orthogonal in
relation to the longitudinal surfaces of external surface 810, or
either one of ends 807 or 809 may be beveled while the other one of
ends 807 or 809 is orthogonal.
[0132] In the depicted embodiment, lumen 805 includes a
longitudinal rib 813. While in the depicted embodiment, the rib 813
extends continuously from first end 807 to second end 809, in some
embodiments, rib 813 may be made of multiple individually shorter
segments and/or other arrangements. It should be understood that
lumen 805 may be configured with any of the lumenal constructs
provided herein (e.g., FIGS. 15-26, and others), and combinations
thereof.
[0133] In the depicted embodiment, second end 809 includes a first
flange portion 814a and a second flange portion 814b. In some
implementations, one or more surfaces of flange portions 814a and
814b contact the surface of the cornea and provide mechanical
stabilization of device 800 in relation to the eye. The outer
lateral surfaces of flange portions 814a and 814b are planar and
parallel to the longitudinal surfaces of external surface 810 in
the depicted embodiment. In some embodiments, the outer lateral
surfaces of flange portions 814a and 814b are contoured. In some
embodiments, the outer lateral surfaces of flange portions 814a and
814b are planar and unparallel or askew in relation to the
longitudinal surfaces of external surface 810.
[0134] In some embodiments, one or more suture attachment features
are included on device 800 (and the other devices provided herein).
In the depicted embodiment, second end 809 includes a first suture
attachment structure 816a and a second suture attachment structure
816b. The suture attachment structures 816a and 816b are holes in
the depicted embodiment. In some embodiments, other types of suture
attachment structures can be alternatively or additionally
included. While the depicted embodiment includes two suture
attachment structures 816a and 816b, in some embodiments, zero,
one, three, four, or more than four suture attachment structures
are included.
[0135] One or more portions of external surface 810 can be
configured for enhanced friction with eye tissue (e.g., the cornea
or sclera). Advantageous mechanical stability and/or migration
resistance of the device 800 (and the other devices provided
herein) in relation to the eye can be facilitated by such portions.
For example, in the depicted embodiment, a plurality of protrusions
818 provide an enhanced texture (greater roughness) in comparison
to other portions of external surface 810. In the depicted
embodiment, protrusions 818 are disposed on opposing surfaces of
external surface 810. It should be understood that protrusions 818
can be located in any desired location(s) on external surface 810.
In some embodiments, other types of texturing configurations can be
alternatively or additionally included. For example, such texturing
configurations can include, but are not limited to, cross-hatching,
stippling, knurling, inclusion of one or more barbs, and the like,
and combinations thereof. In some embodiments, the surface portion
818 is created by techniques such as, but not limited to, laser
machining, plasma etching, chemical etching, 3D printing, photo
etching, and the like.
[0136] Referring to FIGS. 13 and 14, another example device 900 in
accordance with some embodiments provided herein is illustrated.
Device 900 includes a body 903 that defines a lumen 905. Body 903
includes a first end 907 and a second end 909. Body 903 has an
external surface 910 and a lumenal surface 912.
[0137] Device 900 can be constructed using any of the materials and
techniques as described herein in reference to device 1. Also,
device 900 can be configured and used in any of the manners
described herein in reference to device 1.
[0138] In the depicted embodiment, first end 907 is not beveled.
Rather, first end 907 is generally orthogonal in relation to the
longitudinal surfaces of external surface 910. Second end 909 of
the depicted embodiment is beveled in relation to the longitudinal
surfaces of external surface 910. It should be understood that, in
some embodiments of device 900 (and the other devices provided
herein), both ends 907 and 909 may be beveled (e.g., like second
end 909), both ends 907 and 909 may be orthogonal (e.g., like first
end 907), or either one of ends 907 or 909 may be beveled while the
other one of ends 907 or 909 is orthogonal.
[0139] In the depicted embodiment, lumen 905 includes a first
longitudinal rib 913a and a second longitudinal rib 913b. While in
the depicted embodiment, the ribs 913a and 913b extend continuously
from first end 907 to second end 909, in some embodiments, ribs
913a and 913b may be made of multiple individually shorter segments
and/or other arrangements. It should be understood that lumen 905
may be configured with any of the lumenal constructs provided
herein (e.g., FIGS. 15-26, and others), and combinations
thereof.
[0140] In the depicted embodiment, second end 909 includes a first
flange portion 914a and a second flange portion 914b. In some
implementations, flange portions 914a and 914b contact the surface
of the cornea and provide mechanical stabilization of device 900 in
relation to the eye. The outer lateral surfaces of flange portions
914a and 914b are planar and parallel to the longitudinal surfaces
of external surface 910 in the depicted embodiment. In some
embodiments, the outer lateral surfaces of flange portions 914a and
914b are nonplanar (e.g., radiused, chamfered, contoured, etc.). In
some embodiments, the outer lateral surfaces of flange portions
914a and 914b are planar and unparallel or askew in relation to the
longitudinal surfaces of external surface 910.
[0141] In some embodiments, one or more suture attachment features
are included on device 900 (and the other devices provided herein).
In the depicted embodiment, second end 909 includes a first suture
attachment structure 916a and a second suture attachment structure
916b. The suture attachment structures 916a and 916b are slots in
the depicted embodiment. In some embodiments, other types of suture
attachment structures can be alternatively or additionally
included. While the depicted embodiment includes two suture
attachment structures 916a and 916b, in some embodiments, zero,
one, three, four, or more than four suture attachment structures
are included.
[0142] One or more portions of external surface 910 can be
configured for enhanced friction with eye tissue (e.g., the cornea
or sclera). Advantageous mechanical stability and/or migration
resistance of the device 900 (and the other devices provided
herein) in relation to the eye can be facilitated by such portions.
For example, in the depicted embodiment, one or more lateral barbs
918 are included on opposing surfaces of external surface 910. In
the depicted embodiment, lateral barbs 918 are triangular
protrusions with atraumatic tips (e.g., truncated tips, radiused
tips, and the like). In some embodiments, no such lateral barbs 918
are included. In some embodiments, other types of texturing
configurations can be alternatively or additionally included. For
example, such texturing configurations can include, but are not
limited to, stippling, knurling, cross-hatching, and the like, and
combinations thereof. In some embodiments, the surface portion 918
is created by techniques such as, but not limited to, laser
machining, chemical etching, plasma etching, 3D printing, photo
etching, and the like.
[0143] FIGS. 15-26 depict various example lumenal structures that
can be incorporated in the devices provided herein. It should be
understood that the lumenal structures depicted are not an
exhaustive compilation of structures that can be used for
configuring the lumenal passageways of the devices provided herein.
Moreover, the features of one or more of the depicted lumenal
structures can be combined with the features of one or more other
depicted lumenal structures to create many different combinations,
which are within the scope of this disclosure.
[0144] The example lumenal structures can be sized and configured
to provide an appropriate outflow resistance to modulate aqueous
humor flowing through the lumen without the need for an element
that provides additional flow resistance (e.g., a filter or a
porous element). In doing so, the lumen functions to maintain a
desired IOP to treat a glaucoma afflicted eye, while also providing
moisture and lubrication to the surface of eye and tear film. In
some embodiments, a filter or filter-like porous element is
included in the devices provided herein.
[0145] Referring to FIG. 15, an example device 1000 can include a
lumenal structure 1005 that includes one or more longitudinal ribs
1013. In the depicted embodiment, eight longitudinal ribs 1013 are
included. In some embodiments, zero, one, two, three, four, five,
six, seven, nine, ten, eleven, twelve, or more than twelve
longitudinal ribs 1013 are included. Such longitudinal ribs 1013
serve to divide overall lumen 1005 into two or more longitudinal
portions.
[0146] Referring to FIG. 16, an example device 1100 can include a
lumenal structure 1105 that includes one or more longitudinal rib
portions 1113. Such longitudinal rib portions 1113 serve to divide
overall lumen 1105 into some segments having two or more
longitudinal portions, and some segments that are undivided by
longitudinal rib portions 1113. In the depicted embodiment, eight
longitudinal rib portions 1113 are included. In some embodiments,
zero, one, two, three, four, five, six, seven, nine, ten, eleven,
twelve, or more than twelve longitudinal rib portions 1113 are
included. Any suitable number of groupings of longitudinal rib
portions 1113 can be included.
[0147] Referring to FIG. 17, an example device 1200 can include a
lumenal structure 1205 that includes one or more longitudinal rib
portions 1213. Such longitudinal rib portions 1213 serve to divide
overall lumen 1205 into some segments having two or more
longitudinal portions, and some segments that are undivided by
longitudinal rib portions 1213. In addition, in the depicted
embodiment, alternating groupings of longitudinal rib portions 1213
are laterally offset from adjacent groupings of longitudinal rib
portions 1213. In the depicted embodiment, eight longitudinal rib
portions 1213 are included. In some embodiments, zero, one, two,
three, four, five, six, seven, nine, ten, eleven, twelve, or more
than twelve longitudinal rib portions 1213 are included. Any
suitable number of groupings of longitudinal rib portions 1213 can
be included.
[0148] Referring to FIG. 18, an example device 1300 can include a
lumenal structure 1305 that includes one or more longitudinal ribs
1313. In the depicted embodiment, six longitudinal ribs 1313 are
included. In some embodiments, zero, one, two, three, four, five,
seven, eight, nine, ten, eleven, twelve, or more than twelve
longitudinal ribs 1313 are included. Such longitudinal ribs 1313
serve to divide overall lumen 1305 into two or more longitudinal
portions. Longitudinal ribs 1313 can be made to have any suitable
width.
[0149] Referring to FIG. 19, an example device 1400 can include a
lumenal structure 1405 that includes one or more longitudinal rib
portions 1413. Such longitudinal rib portions 1413 serve to divide
overall lumen 1405 into some segments having two or more
longitudinal portions, and some segments that are undivided by
longitudinal rib portions 1413. In the depicted embodiment, six
longitudinal rib portions 1413 are included. In some embodiments,
zero, one, two, three, four, five, seven, eight, nine, ten, eleven,
twelve, or more than twelve longitudinal rib portions 1413 are
included. Any suitable number of groupings of longitudinal rib
portions 1413 can be included. Longitudinal ribs 1313 can be made
to have any suitable width.
[0150] Referring to FIG. 20, an example device 1500 can include a
lumenal structure 1505 that includes one or more longitudinal rib
portions 1513. Such longitudinal rib portions 1513 serve to divide
overall lumen 1505 into some segments having two or more
longitudinal portions, and some segments that are undivided by
longitudinal rib portions 1513. In addition, in the depicted
embodiment, alternating groupings of longitudinal rib portions 1513
are laterally offset from adjacent groupings of longitudinal rib
portions 1513. In the depicted embodiment, six longitudinal rib
portions 1513 are included. In some embodiments, zero, one, two,
three, four, five, seven, nine, eight, ten, eleven, twelve, or more
than twelve longitudinal rib portions 1513 are included. Any
suitable number of groupings of longitudinal rib portions 1513 can
be included. Longitudinal ribs 1313 can be made to have any
suitable width.
[0151] Referring to FIG. 21, an example device 1600 can include a
lumenal structure 1605 that includes one or more longitudinal ribs
1613. In the depicted embodiment, three longitudinal ribs 1613 are
included. In some embodiments, zero, one, two, four, five, six,
seven, eight, nine, ten, eleven, twelve, or more than twelve
longitudinal ribs 1613 are included. Such longitudinal ribs 1613
serve to divide overall lumen 1605 into two or more longitudinal
portions. Longitudinal ribs 1613 can be made to have any suitable
width.
[0152] Referring to FIG. 22, an example device 1700 can include a
lumenal structure 1705 that includes one or more longitudinal rib
portions 1713. Such longitudinal rib portions 1713 serve to divide
overall lumen 1705 into some segments having two or more
longitudinal portions, and some segments that are undivided by
longitudinal rib portions 1713. In the depicted embodiment, three
longitudinal rib portions 1713 are included. In some embodiments,
zero, one, two, four, five, six, seven, eight, nine, ten, eleven,
twelve, or more than twelve longitudinal rib portions 1713 are
included. Any suitable number of groupings of longitudinal rib
portions 1713 can be included. Longitudinal ribs 1713 can be made
to have any suitable width.
[0153] Referring to FIG. 23, an example device 1800 can include a
lumenal structure 1805 that includes one or more longitudinal rib
portions 1813. Such longitudinal rib portions 1813 serve to divide
overall lumen 1805 into some segments having two or more
longitudinal portions, and some segments that are undivided by
longitudinal rib portions 1813. In addition, in the depicted
embodiment, alternating groupings of longitudinal rib portions 1813
are laterally offset from adjacent groupings of longitudinal rib
portions 1813. In the depicted embodiment, three longitudinal rib
portions 1813 are included. In some embodiments, zero, one, two,
four, five, six, seven, nine, eight, ten, eleven, twelve, or more
than twelve longitudinal rib portions 1813 are included. Any
suitable number of groupings of longitudinal rib portions 1813 can
be included. Longitudinal ribs 1313 can be made to have any
suitable width.
[0154] Referring to FIG. 21, an example device 1900 can include a
lumenal structure 1905 that includes a plurality of circular
pillars 1913. Such circular pillars 1913 serve to constrict lumen
1905 but not prevent all flow of fluid through lumen 1905. Circular
pillars 1913 can be made to have any suitable size (e.g.,
diameter). In the depicted embodiment, circular pillars 1913 are
longitudinally aligned in rows.
[0155] Referring to FIG. 22, an example device 2000 can include a
lumenal structure 2005 that includes a plurality of circular
pillars 2013. Such circular pillars 2013 serve to constrict lumen
2005 but not prevent all flow of fluid through lumen 2005. Circular
pillars 2013 can be made to have any suitable size (e.g.,
diameter). In the depicted embodiment, circular pillars 2013 are
laterally offset from longitudinally adjacent circular pillars
2013.
[0156] Referring to FIG. 23, an example device 2100 can include a
lumenal structure 2105 that includes a plurality of ovular pillars
2113. Such ovular pillars 2113 serve to constrict lumen 2105 but
not prevent all flow of fluid through lumen 2105. Ovular pillars
2113 can be made to have any suitable size (e.g., length and
width). In the depicted embodiment, ovular pillars 2113 are
laterally offset from longitudinally adjacent ovular pillars
2113.
[0157] Referring to FIGS. 27 and 28, another example device 2200 in
accordance with some embodiments provided herein is illustrated.
Device 2200 includes a body 2203 that defines a lumen 2205. Body
2203 includes a first end 2207 and a second end 2209. Body 2203 has
an external surface 2210, and a lumenal surface 2212. Device 2200
also includes a bolster portion 2204. Bolster portion 2204 can be
mated with body 2203. In some cases, second end 2209 of body 2203
can be coupled with receptacle 2218 of bolster portion 2204. In
some embodiments, a compression fit (interference fit) exists
between body 2203 and bolster portion 2204, such that body 2203 and
bolster portion 2204 are held together and effectively function as
a monolithic device prior to and after implantation into an
eye.
[0158] Bolster portion 2204 and body 2203 can be constructed using
any of the materials and techniques as described herein in
reference to device 1. In addition, in some embodiments, bolster
portion 2204, or portions thereof, is made of silicone. In some
embodiments, bolster portion 2204, or portions thereof, is made of
PET. Device 2200 can be configured and used in any of the manners
described herein in reference to device 1.
[0159] Bolster portion 2204 provides a stable footing for device
2200 when device 2200 is implanted in an eye. In some cases, at
least a portion of bolster portion 2204 contacts the surface of the
eye, thereby mechanically stabilizing the device 2200 in relation
to the eye. In some cases, bolster portion 2204 can serve to
prevent or inhibit tipping of device 2200 in relation to the eye.
Other device design features and device use techniques to prevent
or inhibit tipping of device 2200 (and the other devices provided
herein) in relation to the eye are also envisioned. For example,
the inclusion of design features such as barbs, textured surfaces,
projections, and other mechanical aspects can be included to
prevent or inhibit tipping. Further, in some cases the angle of
insertion of the device 200 (and the other devices provided herein)
can be selected and/or optimized so prevent or inhibit tipping.
[0160] While in the depicted embodiment, bolster portion 2204 is
rectangular, in some embodiments, bolster portions with other
shapes are used. Such shapes can include, but are not limited to,
circles, ovals, squares, parallelograms, and the like. Bolster
portion 2219 can be oriented at an angle 2219 in relation to body
2203. In some embodiments, angle 2219 is about a 45.degree. angle.
In some embodiments, angle 2219 is within the range from about
40.degree. to about 50.degree., or from about 35.degree. to about
45.degree., or from about 45.degree. to about 55.degree., or from
about 30.degree. to about 60.degree., or from about 20.degree. to
about 70.degree., or from about 10.degree. to about 80.degree., or
from about 0.degree. to about 90.degree., or greater than about
90.degree..
[0161] In the depicted embodiment, first end 2207 is beveled. In
some embodiments, first end 2207 is generally orthogonal in
relation to the longitudinal surfaces of external surface 2210.
Second end 2209 of the depicted embodiment is not beveled in
relation to the longitudinal surfaces of external surface 2210. It
should be understood that, in some embodiments of device 2200 and
the other devices provided herein, both ends 2207 and 2209 may be
beveled (e.g., like first end 2207), both ends 2207 and 2209 may be
orthogonal (e.g., like second end 2209), or either one of ends 2207
or 2209 may be beveled while the other one of ends 2207 or 2209 is
orthogonal.
[0162] In the depicted embodiment, second end 2209 extends beyond
bolster portion 2204. In some embodiments, second end 2209 is flush
or slightly recessed in relation to bolster portion 2204.
[0163] In the depicted embodiment, lumen 2205 includes a
longitudinal rib 2213. While in the depicted embodiment, rib 2213
extends continuously from first end 2207 to second end 2209, in
some embodiments, rib 2213 may be made of multiple individually
shorter segments and/or other arrangements. It should be understood
that lumen 2205 may be configured with any of the lumenal
constructs provided herein (e.g., FIGS. 15-26, and others), and
combinations thereof.
[0164] In the depicted embodiment, second end 2209 includes a first
flange portion 2214a and a second flange portion 2214b. In some
implementations, flange portions 2214a and 2214b contact the
surface of the cornea and provide mechanical stabilization of
device 2200 in relation to the eye. In addition, in this two-piece
construct of device 2200, flange portions 2214a and 2214b engage
within recesses of bolster portion 2204 to provide a sturdy
mechanical connection therebetween. In the depicted embodiment,
flange portions 2214a and 2214b protrude from bolster portion 2204.
In some embodiments, flange portions 2214a and 2214b are flush or
slightly recessed in relation to bolster portion 2204.
[0165] In some embodiments, one or more suture attachment features
are included on device 2200 (and the other devices provided
herein). In the depicted embodiment, bolster portion 2204 includes
a first suture attachment structure 2216a and a second suture
attachment structure 2216b. The suture attachment structures 2216a
and 2216b are holes in the depicted embodiment. In some
embodiments, other types of suture attachment structures can be
alternatively or additionally included. While the depicted
embodiment includes two suture attachment structures 2216a and
2216b, in some embodiments, zero, one, three, four, or more than
four suture attachment structures are included.
[0166] One or more portions of external surface 2210 can be
configured for enhanced friction with eye tissue (e.g., the cornea
or sclera) to improve mechanical stability and/or migration
resistance of the device 2200 (and the other devices provided
herein) in relation to the eye. In some embodiments, configurations
of external surface 2210 can include, but are not limited to,
stippling, knurling, cross-hatching, inclusion of one or more
barbs, and the like, and combinations thereof. In some embodiments,
some such configurations are created by techniques such as, but not
limited to, laser machining, chemical etching, plasma etching, 3D
printing, photo etching, and the like.
[0167] Referring to FIGS. 29 and 30, another example device 2300 in
accordance with some embodiments provided herein is illustrated.
Device 2300 includes a body 2303 that defines a lumen 2305. Body
2303 includes a first end 2307 and a second end 2309. Body 2303 has
an external surface 2310 and a lumenal surface 2312. Device 2300
also includes a bolster portion 2304. Bolster portion 2304 can be
mated with body 2303. In some cases, body 2303 can be coupled with
receptacle 2318 of bolster portion 2304 such that flange portions
2314a and 2314b are positioned in contact with bolster portion
2304. In some embodiments, a compression fit (interference fit)
exists between body 2303 and bolster portion 2304, such that body
2303 and bolster portion 2304 are held together and effectively
function as a monolithic device prior to and after implantation
into an eye.
[0168] Bolster portion 2304 and body 2303 can be constructed using
any of the materials and techniques as described herein in
reference to device 1. In addition, in some embodiments, bolster
portion 2304, or portions thereof, is made of silicone. In some
embodiments, bolster portion 2304, or portions thereof, is made of
PET. Device 2300 can be configured and used in any of the manners
described herein in reference to device 1.
[0169] Bolster portion 2304 provides a stable footing for device
2300 when device 2300 is implanted in an eye. In some cases, at
least a portion of bolster portion 2304 contacts the surface of the
eye, thereby mechanically stabilizing the device 2300 in relation
to the eye. In some cases, bolster portion 2304 can serve to
prevent or inhibit tipping of device 2300 in relation to the
eye.
[0170] While in the depicted embodiment, bolster portion 2304 is
ovular, in some embodiments, bolster portions with other shapes are
used. Such shapes can include, but are not limited to, circles,
rectangles, squares, parallelograms, and the like. Bolster portion
2319 can be oriented at an angle 2319 in relation to body 2303. In
some embodiments, angle 2319 is about a 45.degree. angle. In some
embodiments, angle 2319 is within the range from about 40.degree.
to about 50.degree., or from about 35.degree. to about 45.degree.,
or from about 45.degree. to about 55.degree., or from about
30.degree. to about 60.degree., or from about 20.degree. to about
70.degree., or from about 10.degree. to about 80.degree., or from
about 0.degree. to about 90.degree., or greater than about
90.degree..
[0171] In the depicted embodiment, first end 2307 is not beveled.
Rather, first end 2307 is generally orthogonal in relation to the
longitudinal surfaces of external surface 2310. Second end 2309 of
the depicted embodiment is also not beveled in relation to the
longitudinal surfaces of external surface 2310. It should be
understood that, in some embodiments of device 2300 and the other
devices provided herein, both ends 2307 and 2309 may be beveled,
both ends 2307 and 2309 may be orthogonal, or either one of ends
2307 or 2309 may be beveled while the other one of ends 2307 or
2309 is orthogonal.
[0172] In the depicted embodiment, second end 2309 extends beyond
bolster portion 2304. In some embodiments, second end 2309 is flush
or slightly recessed in relation to bolster portion 2304.
[0173] In the depicted embodiment, lumen 2305 includes a
longitudinal rib 2313. While in the depicted embodiment, rib 2313
extends continuously from first end 2307 to second end 2309, in
some embodiments, rib 2313 may be made of multiple individually
shorter segments and/or other arrangements. It should be understood
that lumen 2305 may be configured with any of the lumenal
constructs provided herein (e.g., FIGS. 15-26, and others), and
combinations thereof.
[0174] In the depicted embodiment, second end 2309 includes first
flange portion 2314a and second flange portion 2314b. In this
two-piece construct of device 2300, flange portions 2314a and 2314b
engage with bolster portion 2304 to provide a sturdy mechanical
connection therebetween. In the depicted embodiment, flange
portions 2314a and 2314b protrude from bolster portion 2304. In
some embodiments, flange portions 2314a and 2314b are flush or
slightly recessed in relation to bolster portion 2304.
[0175] In some embodiments, one or more suture attachment features
are included on device 2300 (and the other devices provided
herein). In the depicted embodiment, bolster portion 2304 does not
include any such suture attachment features. In some embodiments,
when bolster portion 2304 is made of silicone, bolster portion 2304
can be pierced by a needle to allow sutures to be threaded through
bolster portion 2304 (despite the lack of specific suture
attachment features). While the depicted embodiment includes no
suture attachment structures, in some embodiments, one, two, three,
four, or more than four suture attachment structures are
included.
[0176] One or more portions of external surface 2310 can be
configured for enhanced friction with eye tissue (e.g., the cornea
or sclera) to improve mechanical stability and/or migration
resistance of the device 2300 (and the other devices provided
herein) in relation to the eye. In some embodiments, configurations
of external surface 2310 can include, but are not limited to,
stippling, knurling, cross-hatching, inclusion of one or more
barbs, and the like, and combinations thereof. In some embodiments,
some such configurations are created by techniques such as, but not
limited to, laser machining, chemical etching, 3D printing, plasma
etching, photo etching, and the like.
[0177] Referring to FIG. 31, an example device 2400 is shown
implanted in afflicted eye 20 for the purpose of treating glaucoma
and/or dry eye of afflicted eye 20. The depicted anatomical
features of eye 20 include anterior chamber 2, sclera 6, tear film
4, iris 23, ciliary body 25, and cornea 21.
[0178] Device 2400 includes body 2403 that defines lumen 2405. Body
2403 includes first end 2407 and a second end 2409. Body 2403 has
an external surface 2410, and a lumenal surface 2412.
[0179] In the depicted embodiment, device 2400 also includes a
longitudinal extension member 2420 that is attached to body 2403.
An anchor member 2422 is attached to the opposite end of the
extension member 2420. Anchor member 2422 can be a structure such
as, but not limited to, a barb, a hook, a screw, a clamp, and the
like. Anchor member 2422 can be implanted within or attached to
cornea 21 or sclera 6. In some cases, extension member 2420 and
anchor member 2422 serve to stabilize mechanically device 2400 in
relation to eye 20.
[0180] In some embodiments, extension member 2420 is a wire member,
or another type of elongate member. In some embodiments, extension
member 2420 and anchor member 2422 are made of a metallic material
such as nitinol or stainless steel. Alternatively or additionally,
in some embodiments, extension member 2420 and anchor member 2422
are made of a polymeric material.
[0181] Referring to FIG. 32, another example device 2500 in
accordance with some embodiments provided herein is illustrated.
Device 2500 includes a body 2503 that defines a lumen 2505. Body
2503 includes a first end 2507 and a second end 2509. Body 2503 has
an external surface 2510 and a lumenal surface 2512.
[0182] Device 2500 can be constructed using any of the materials
and techniques as described herein in reference to device 1. Also,
device 2500 can be configured and used in any of the manners
described herein in reference to device 1.
[0183] In the depicted embodiment, first end 2507 is beveled. In
some embodiments, first end 2507 is generally orthogonal in
relation to the longitudinal surfaces of external surface 2510.
Second end 2509 of the depicted embodiment is not beveled in
relation to the longitudinal surfaces of external surface 2510. It
should be understood that, in some embodiments of device 2500 and
the other devices provided herein, both ends 2507 and 2509 may be
beveled (e.g., like first end 2507), both ends 2507 and 2509 may be
orthogonal (e.g., like second end 2509), or either one of ends 2507
or 2509 may be beveled while the other one of ends 2507 or 2509 is
orthogonal.
[0184] In the depicted embodiment, lumen 2505 is open continuously
from first end 2507 to second end 2509. In some embodiments, lumen
2505 can be configured with any of the other lumenal constructs
provided herein (e.g., FIGS. 15-26, and others), and combinations
thereof.
[0185] In the depicted embodiment, second end 2509 includes a first
flange portion 2514a and a second flange portion 2514b. In some
implementations, flange portions 2514a and 2514b contact the
surface of the cornea and provide mechanical stabilization of
device 2500 in relation to the eye. The outer lateral surfaces of
flange portions 2514a and 2514b are radiused (contoured) in the
depicted embodiment. In some embodiments, the outer lateral
surfaces of flange portions 2514a and 2514b are planar and parallel
to the longitudinal surfaces of external surface 2510. In some
embodiments, the outer lateral surfaces of flange portions 2514a
and 2514b are planar and unparallel or askew in relation to the
longitudinal surfaces of external surface 2510.
[0186] In some embodiments, one or more suture attachment features
are included on device 2500 (and the other devices provided
herein). In the depicted embodiment, second end 2509 includes a
first suture attachment structure 2516a and a second suture
attachment structure 2516b. The suture attachment structures 2516a
and 2516b are grooves in the depicted embodiment. In some
embodiments, other types of suture attachment structures can be
alternatively or additionally included. While the depicted
embodiment includes two suture attachment structures 2516a and
2516b, in some embodiments, zero, one, three, four, or more than
four suture attachment structures are included.
[0187] One or more portions of external surface 2510 can be
configured for enhanced friction with eye tissue (e.g., the cornea
or sclera). Advantageous mechanical stability and/or migration
resistance of the device 2500 (and the other devices provided
herein) in relation to the eye can be facilitated by such portions.
For example, in the depicted embodiment, a surface portion 2518
includes an enhanced texture (roughness) in comparison to other
portions of external surface 2510. In the depicted embodiment,
surface portion 2518 is a stippled surface. In some embodiments,
other types of texturing configurations can be alternatively or
additionally included. For example, such texturing configurations
can include, but are not limited to, cross-hatching, knurling,
inclusion of one or more barbs, and the like, and combinations
thereof. In some embodiments, the surface portion 2518 is created
by techniques such as, but not limited to, laser machining, plasma
etching, chemical etching, 3D printing, photo etching, and the
like.
[0188] Referring to FIG. 33, another example device 2600 in
accordance with some embodiments provided herein is illustrated.
Device 2600 includes a body 2603 that defines a lumen 2605. Body
2603 includes a first end 2607 and a second end 2609. Body 2603 has
an external surface 2610, and a lumenal surface 2612.
[0189] Device 2600 can be constructed using any of the materials
and techniques as described herein in reference to device 1. Also,
device 2600 can be configured and used in any of the manners
described herein in reference to device 1.
[0190] In the depicted embodiment, device 2600 is generally
configured in the arrangement as device 2500 of FIG. 32. Device
2600 differs from device 2500 in that second end 2609 is extended
beyond flange portions 2614a and 2614b by a distance 2620. In some
embodiments, distance 2620 is about 300 .mu.m. In some embodiments,
distance 2620 is in a range from about 200 .mu.m to about 400
.mu.m, or from about 100 .mu.m to about 500 .mu.m, or from about 0
.mu.m to about 600 .mu.m.
[0191] Referring to FIG. 34, example devices 2700 and 2800 can be
implanted in an eye 20 that is afflicted with glaucoma.
[0192] A second method for installing the devices provided herein
is as follows. Sometime before installation, the eye is irrigated
with 1-5% Betadine solution, and topical antibiotic and
non-steroidal anti-inflammatory drops (NSAID) are applied to the
operative eye. These can be continued for about one week
postoperatively four times a day. The NSAID can help stabilize the
blood-aqueous barrier. All embodiments of the device illustrated
herein may be inserted under topical anesthesia, possibly
supplemented subconjunctivally.
[0193] This insertion procedure can be conducted without excising
conjunctiva at the site of the anticipated insertion. Approximately
1-2 mm posterior to the limbus, a diamond blade can be used to make
a stab incision into the anterior chamber, while held roughly
parallel to the iris. The blade can be of a size predetermined to
make an opening into the anterior chamber sized appropriately for
the introduction of the device. This stab incision can be made
gently, but relatively quickly, assiduously avoiding any and all
intraocular structures.
[0194] The device is next picked up and can be held with a
non-toothed forceps. The lips of the stab incision wound may be
gaped with a fine, toothed forceps. The distal end (which may or
may not be a pointed/beveled tip) of the tube element would then be
gently pushed through the scleral tract of the stab incision and
into the anterior chamber, with the device lying above and parallel
to the iris, with the bevel up (i.e., anteriorly). The lateral
flanges in the embodiments so configured provide for a definite
endpoint to the depth of insertion. For embodiments of the device
having a beveled first end, the bevel is oriented anteriorly to
minimize the potential for blockage of the lumenal opening by the
iris. The scleral barb(s) or other outer surface features (if
included) can stabilize the device until the biointegration with
the sclera is complete. This biointegration is a function of its
porous cellular ingrowth surface, possibly enhanced by adsorbed
growth factors and/or grafted extracellular matrix proteins. In
some implementations, one or more sutures may be added using the
device's suture attachment features to stabilize the device prior
to biointegration. For example, a 10-0 nylon suture on a broad
spatula needle may be used to suture the device the sclera,
providing additional stability to the device until the
biointegration is complete. This suture may then be easily removed
at a later time if needed. An alternative insertion technique can
include having the device pre-loaded into an insertion holder or
cartridge, to limit the needed handling of the device by the
surgeon. A properly sized sharp blade could be at the leading edge
of the inserter, such blade acting also as a guide for implanting
the device. Alternatively, the paracentesis can be made with a
separate blade, followed by controlled insertion with an
inserter.
[0195] After insertion of the device, an ocular shield can be
placed over the eye. The implanted device can bio-integrate with
the sclera, thereby reducing the risks of infections such as tunnel
infection.
[0196] Referring to FIG. 35, eye 20 is shown after devices 2700 and
2800 have been implanted for a period of approximately two weeks.
The end portions of devices 2700 and 2800 have not been overgrown
with conjunctival tissue. Hence, the lumens of devices 2700 and
2800 are patent and can function to reduce IOP, thereby treating
glaucoma in a safe and effective manner.
[0197] Referring to FIG. 36, eye 20 is shown after devices 2700 and
2800 have been implanted for a period of approximately one month.
The end portions of devices 2700 and 2800 still have not been
overgrown with conjunctival tissue. Hence, the lumens of devices
2700 and 2800 are patent and can function to reduce IOP, thereby
treating glaucoma in a safe and effective manner. In addition, the
photo shows that the prior irritation (redness) of the tissue has
subsided. Hence, devices 2700 and 2800 have been successfully
integrated by the patient in this example.
[0198] Prevention of conjunctival tissue overgrowth to sustain
patency of the device's lumen has been found to be effected by a
number of various design factors such as, but not limited to,
material selection, coatings, physical distance and geometry of the
projection of the device from the surface of the eye, and the angle
of the projecting end relative to the eye. For example, from animal
experimentation, the relationships between time and projection
distance (distance from the eye's surface to the end of the device)
shown in Table 1 below have been observed.
TABLE-US-00001 TABLE 1 Amount of Conjunctival Overgrowth 1 Week 2
Weeks 1 Month 2 Months Projection after after after after Distance
Implantation Implantation Implantation Implantation 200 .mu.m none
partial full full 800 .mu.m none none none none
[0199] Referring to FIGS. 37 and 38, another example device for
treating glaucoma and/or dry eye in accordance with the techniques
provided herein is a two-piece device 2900. Two-piece device 2900
includes a collar 2910 and a cartridge 2940. Collar 2910 is
configured to slidably receive cartridge 2940, such that collar
2910 and cartridge 2940 are releasably coupleable.
[0200] During normal use, collar 2910 and cartridge 2940 are
coupled together (as shown in FIG. 38). In that coupled
arrangement, two-piece device 2900 can be implanted in a sclera of
an afflicted eye to allow aqueous humor to flow from the anterior
chamber of the afflicted eye through two-piece device 2900, and
into the tear film (as shown in FIG. 39). This outflow of aqueous
humor into the tear film can treat glaucoma by reducing the
intraocular pressure of the afflicted eye, in addition to providing
moisture and lubrication to the surface of the eye. Such
functionality is consistent with that of other device embodiments
described herein.
[0201] Along with the ability to reduce intraocular pressure,
two-piece device 2900 provides added functional advantages related
to the fact that collar 2910 and cartridge 2940 are releasably
coupleable. For example, as described further herein, while collar
2910 remains implanted in the sclera of an afflicted eye, a used
cartridge 2940 can be removed from engagement with the implanted
collar 2910, and a new cartridge 2940 can be reinstalled into the
implanted collar 2910. In some cases, such a procedure for
installing a new cartridge 2940 is not as extensive as would be the
procedure for installing an entire new single piece device. Hence,
two-piece device 2900 can in some cases provide functional
advantages related to the fact that collar 2910 and cartridge 2940
are releasably coupleable.
[0202] Collar 2910 and cartridge 2940 can be constructed using any
of the materials and techniques as described herein in reference to
device 1 and other devices provided herein. In addition, in some
embodiments, collar 2910 and/or cartridge 2940, or portions
thereof, are made of silicone. In some embodiments, collar 2910
and/or cartridge 2940, or portions thereof, are made of PET.
Two-piece device 2900 can be configured and used in any of the
manners described herein in reference to device 1. In some cases,
the inner and/or outer surfaces of the two-piece device 2900 can be
coated with materials such as polymer coatings or biologically
active molecules, to promote surface biocompatibility and/or
immobilization of the implanted device.
[0203] Collar 2910 includes a body 2912. In the depicted
embodiment, body 2912 includes barbs 2912a and 2912b. One or more
portions of body 2912 can be configured for enhanced friction with
eye tissue (e.g., the cornea or sclera). Advantageous mechanical
stability and/or migration resistance of the device two-piece 2900
(and the other devices provided herein) in relation to the eye can
be facilitated by such portions. For example, in the depicted
embodiment, one or more lateral barbs 2912a and 2912b are included
on opposing surfaces of body 2912. In the depicted embodiment,
lateral barbs 2912a and 2912b are triangular protrusions with sharp
tips. Other types of shapes may be used for lateral barbs 2912a and
2912b. In some embodiments, lateral barbs 2912a and 2912b are
configured to be atraumatic (e.g., truncated tips, radiused tips,
and the like). In some embodiments, multiple barbs are used on one
or more particular surfaces of body 2912. In some embodiments, no
such lateral barbs 2912a and 2912b are included. The barbs 2912a
and 2912b may be formed as part of body 2912 during manufacture, or
may be fused or bonded to body 2912 using any appropriate
technique.
[0204] In the depicted embodiment, a surface portion 2918 of body
2912 includes an enhanced texture (roughness) in comparison to
other surface portions of body 2912. In the depicted embodiment,
surface portion 2918 is a cross-hatched surface. In some
embodiments, other types of texturing configurations can be
alternatively or additionally included. For example, such texturing
configurations can include, but are not limited to, stippling,
knurling, inclusion of one or more barbs, and the like, and
combinations thereof. In some embodiments, the surface portion 2918
is created by techniques such as, but not limited to, laser
machining, chemical etching, plasma etching, 3D printing, photo
etching, and the like. Such texturing can be located on all
external surfaces of body 2912 in some embodiments. In specific
embodiments, texturing may be located on some external surfaces of
body 2912, but not on others. In some embodiments, no such
texturing is included on any external surfaces of body 2912.
[0205] Body 2912 defines a lumen 2914. Lumen 2914 can extend
entirely through body 2912 from a proximal end to a distal end of
body 2912. In some embodiments, lumen 2914 is sized for press-fit
coupling with cartridge 2940. That is, in some embodiments a
dimensional interference between the sizes of lumen 2914 and
cartridge 2940 may facilitate a mechanical coupling therebetween.
Alternatively, or additionally, in some embodiments other
mechanical coupling techniques between body 2914 and cartridge 2940
can be used. Such techniques can include, but are not limited to,
use of adhesives, snap-fitting, use of welding techniques,
threading, clamping, and the like, and combinations thereof.
[0206] PEG can be used to define lumen 2914, in some embodiments.
The use of PEG for the surfaces of lumen 2914 can be advantageous
because PEG resists bacterial, protein, and cell adherence. In some
embodiments, low molecular weight PEG can be used. In some cases,
the PEG is photo-polymerized. In some cases, the PEG is not
photo-polymerized.
[0207] In order to facilitate a desired coupling arrangement
between cartridge 2940 and lumen 2914, in some embodiments the
outer dimensions of cartridge 2940 are inconsistent along the
longitudinal length of cartridge 2940. For example, in some
embodiments a distal portion of cartridge 2940 has smaller outer
dimensions than a proximal portion of cartridge 2940. That way,
when cartridge 2940 is inserted into lumen 2914, the distal portion
of cartridge 2940 will slide through lumen 2914, while the proximal
portion of cartridge 2940 will become coupled with lumen 2914 due
to a dimensional interference therebetween.
[0208] Cartridge 2940 includes a body 2943 that defines a lumen
2945. Body 2943 includes a first end 2947 and a second end 2949.
Body 2943 has an external surface 2210, and a lumenal surface 2212.
Device 2200 also includes a bolster portion 2204. Bolster portion
2204 can be mated with body 2203. In some cases, second end 2209 of
body 2203 can be coupled with receptacle 2218 of bolster portion
2204.
[0209] In the depicted embodiment, lumen 2945 includes a
longitudinal rib 2953. While in the depicted embodiment, rib 2953
extends continuously from first end 2947 to second end 2949, in
some embodiments, rib 2953 may be made of multiple individually
shorter segments and/or other arrangements. It should be understood
that lumen 2945 may be configured with any of the lumenal
constructs provided herein (e.g., FIGS. 15-26, and others), and
combinations thereof.
[0210] While in the depicted embodiment, the cross-sectional shapes
of collar 2910 and cartridge 2940 are rectangular, in some
embodiments, other cross-sectional shapes are used. Such
cross-sectional shapes can include, but are not limited to,
circles, ovals, squares, parallelograms, and the like.
[0211] In the depicted embodiment, first end 2947 is not beveled.
Rather, first end 2947 is generally orthogonal in relation to the
longitudinal external surfaces of body 2943. Second end 2949 of the
depicted embodiment is beveled in relation to the longitudinal
external surfaces of body 2943. It should be understood that, in
some embodiments of two-piece device 2900 and the other devices
provided herein, both ends 2947 and 2949 may be beveled, both ends
2947 and 2949 may be orthogonal, or either one of ends 2947 and
2949 may be beveled while the other one of ends 2947 and 2949 is
orthogonal.
[0212] In the depicted embodiment, second end 2949 extends beyond
collar 2910 (in the coupled arrangement of FIG. 38). For example,
in some embodiments second end 2949 extends beyond collar 2910 by
about 200 .mu.m. In some embodiments, second end 2949 extends
beyond collar 2910 by a distance in a range from about 50 .mu.m to
about 1000 .mu.m, or from about 50 .mu.m to about 200 .mu.m, or
from about 100 .mu.m to about 300 .mu.m, or from about 200 .mu.m to
about 400 .mu.m, or from about 300 .mu.m to about 500 .mu.m, or
from about 400 .mu.m to about 600 .mu.m, or from about 500 .mu.m to
about 700 .mu.m, or from about 600 .mu.m to about 800 .mu.m, or
from about 700 .mu.m to about 900 .mu.m, or from about 800 .mu.m to
about 1,000 .mu.m. In some embodiments, while in the coupled
arrangement, second end 2949 is flush or slightly recessed in
relation to collar 2910.
[0213] In some embodiments, one or more suture attachment features
are optionally included on two-piece device 2900 (and the other
devices provided herein). For example, in some embodiments suture
attachment features may be included on collar 2910. The suture
attachment features can be holes, slots, flanges, and the like, and
combinations thereof in the depicted embodiment.
[0214] Referring to FIG. 39, two-piece device 2900 is shown
implanted in an afflicted eye 20 for the purpose of treating
glaucoma and/or dry eye of afflicted eye 20. The depicted
anatomical features of eye 20 include an anterior chamber 2, a
sclera 6, a tear film 4, an iris 23, a ciliary body 25, and a
cornea 21. Two-piece device 2900 includes collar 2910 and cartridge
2940. Cartridge 2940 includes first end 2947 and second end
2949.
[0215] As depicted, two-piece device 2900 is configured to be
surgically implanted in sclera 6 of eye 20. Two-piece device 2900
has a length sufficient to provide fluid communication between
anterior chamber 2 and tear film 4 of eye 20 when two-piece device
2900 is implanted in sclera 6. As described further herein, in some
embodiments, lumen 2945 can be sized and configured to provide an
appropriate outflow resistance to modulate aqueous humor flowing
through lumen 2945, without an element that provides additional
flow resistance (e.g., a filter or a porous element). In doing so,
lumen 2945 functions to maintain a desired IOP to treat a
glaucoma-afflicted eye 20, while also providing moisture and
lubrication to the surface of eye 20 and tear film 4. In other
words, aqueous humor is shunted directly to tear film 4. No
conjunctival bleb is formed. Additionally, no EVP is created that
could raise nocturnal IOP. Rather, EVP is unaffected. In some
cases, lumen 2945 includes a filter or a porous element.
[0216] In some cases, collar 2910 can be implanted so that the
proximal end of collar 2910 is generally flush with the outer
surface of eye 20. Collar 2910 can be configured with a length such
that when generally flush with the outer surface of eye 20, the
distal end of collar 2910 extends beyond sclera 6, just into
anterior chamber 2.
[0217] In some cases, to provide fluid communication between
anterior chamber 2 and tear film 4 (via lumen 2945), two-piece
device 2900 has a total length of about 2.5 mm. In some
embodiments, two-piece device 2900 has a total length of between
about 2.5 mm and about 5.0 mm, or between about 3.5 mm and about
6.0 mm. The length of at least about 2.5 mm will reduce the
possibility of blockage of the lumenal opening in anterior chamber
2 by iris 23. The length of two-piece device 2900 within the
scleral tract would preferably be greater than the scleral
thickness, because insertion would not be perpendicular to sclera 6
(but more tangential) to be parallel to iris 23.
[0218] As described in reference to FIGS. 37 and 38, two-piece
device 2900 is configured such that cartridge 2940 can be removed
from the collar 2910 while collar 2910 remains implanted in sclera
6. Thereafter, a new cartridge 2940 can be readily installed in
collar 2910. Such a feature can be advantageous in various
circumstances. In one example circumstance, over a period of time
lumen 2945 of a used cartridge 2940 may become partially or fully
occluded by biomaterials, for example. Therefore, it may become
desirable or necessary to remove used cartridge 2940, and to
install a new cartridge 2940. In such a case, a clinician can
remove used cartridge 2940 (while leaving collar 2910 in its
implanted position) and then install a new cartridge 2940 into a
coupled arrangement with collar 2910.
[0219] In another example circumstance, two-piece device 2900 is
configured to be adaptable to a patient's needs over time by
facilitating the use of cartridges 2940 of differing flow
resistances in accordance with the patient's needs. For example,
physicians can prescribe different resistance levels if the patient
needs more or less AH flow to treat the patient's glaucoma. When a
cartridge 2940 with a different resistance level is needed by the
patient, the old cartridge 2940 can be removed and the new
cartridge 2940 can be installed, using the advantageous techniques
(while leaving collar 2910 in its implanted position) accommodated
by two-piece device 2900.
[0220] Referring to FIGS. 40 and 41, in some cases a deployment
tool 3000 can be used to assist in the implantation of the glaucoma
and/or dry eye treatment devices provided herein (such as the
depicted example device 3100). The use of deployment tool 3000 can
be advantageous because the minute size of glaucoma and/or dry eye
treatment device 3100 can make glaucoma and/or dry eye treatment
device 3100 otherwise challenging for a clinician to handle and
manipulate as needed during the implantation process.
[0221] Deployment tool 3000 includes a grasping portion 3010, a
shaft 3020, and a distal end 3030 that is configured to releasably
engage with device 3100. In the depicted embodiment, distal end
3030 includes a slot 3032 that is configured to releasably engage
with a proximal end of device 3100. For example, in some
embodiments a light interference fit can be provided between slot
3032 and proximal end of device 3100. In some embodiments, other
releasable engagement techniques between distal end 3030 and device
3100 can be used. For example, in some embodiments distal end 3030
can include retractable tabs that a clinician can retract after
device 3100 has been implanted in the eye of a patient. Other
releasable engagement techniques are also contemplated.
[0222] In some cases, an end user clinician may receive deployment
tool 3000 and device 3100 in a coupled arrangement, in a sterile
package. To perform the implant procedure, the clinician would
remove the coupled combination of deployment tool 300 and device
3100 from the sterile package, and use deployment tool to implant
device 3100 in accordance with the implant techniques described
herein. When device 3100 is implanted in the patient's eye as
desired, the clinician can uncouple deployment tool 3000 from
implanted device 3100.
[0223] Referring to FIGS. 42 and 43, another example device 3200 in
accordance with some embodiments provided herein is illustrated.
Device 3200 includes a body 3203 that defines a lumen 3205 and a
longitudinal axis 3201. Body 3203 includes a distal end portion
3220, a mid-body portion 3240, and a proximal end portion 3260.
Body 3203 includes a distal edge 3222 and a proximal edge 3262.
Body 3203 has an external surface 3210 and a lumenal surface
3212.
[0224] Body 3203 has a maximum longitudinal length L extending
longitudinally between distal edge 3222 and proximal edge 3262.
Body 3203 has lateral widths (e.g., as defined in FIG. 42 by Wd,
Wm, and Wp) extending orthogonally in relation to axis 3201. Body
3203 has a thickness T.
[0225] Device 3200 can be constructed using any of the materials
and techniques as described herein in reference to device 1. Also,
device 3200 can be configured and used in any of the manners
described herein in reference to device 1. Thickness T can be,
without limitation, between about 0.5 mm to about 3.0 mm, or about
0.8 mm to about 2.5 mm, or about 1.0 mm to about 2.0 mm, or about
1.2 mm to about 1.8 mm.
[0226] In the depicted embodiment, lumen 3205 does not include
ribs. In some embodiments, lumen 3205 includes one or more ribs.
Such ribs may extend continuously between distal edge 3222 and
proximal edge 3262, or, in some embodiments, such ribs may be made
of multiple individually shorter segments and/or other
arrangements. It should be understood that lumen 3205 may be
configured with any of the lumenal constructs provided herein
(e.g., FIGS. 15-26, and others), and combinations thereof.
[0227] In the depicted embodiment, distal end portion 3220 includes
a radiused distal edge 3222 having a radius 3224, a first lateral
edge 3226, and a second lateral edge 3228. Radiused distal edge
3222 extends along an arc between first lateral edge 3226 and
second lateral edge 3228. In some cases, a radiused distal edge
3222 can facilitate a less forceful insertion technique as compared
to a non-radiused distal leading edge.
[0228] In the depicted embodiment, radius 3224 is centered on axis
3201 such that body 3203 is symmetrical about axis 3201, but such
centering and axial symmetry is not required in all embodiments. In
some embodiments, radius 3224 is between about 0.2 mm and about 0.8
mm. In some embodiments, without limitation, radius 3224 is between
about 0.2 mm and about 0.6 mm, or about 0.3 mm and about 0.6 mm, or
about 0.4 mm and about 0.6 mm, or about 0.2 mm and about 1.0 mm, or
about 0.2 mm and about 0.9 mm, or about 0.2 mm and about 0.7 mm, or
about 0.2 mm and about 0.5 mm.
[0229] In the depicted embodiment, distal end portion 3220 is
laterally flared. That is, first lateral edge 3226 and second
lateral edge 3228 can each be non-parallel to axis 3201. While in
the depicted embodiment first lateral edge 3226 and second lateral
edge 3228 define equal non-parallel angles 3230 in relation to axis
3201, in some embodiments first lateral edge 3226 and second
lateral edge 3228 define dissimilar non-parallel angles in relation
to axis 3201. In some embodiments, first lateral edge 3226 and/or
second lateral edge 3228 define angle 3230 in relation to axis 3201
at between about 5 degrees and about 30 degrees. In some
embodiments, without limitation, angle 3230 is between about 0
degrees to about 80 degrees, or about 0 degrees to about 60
degrees, or about 0 degrees to about 45 degrees, or about 10
degrees and about 35 degrees, or about 10 degrees and about 25
degrees, or about 10 degrees and about 20 degrees.
[0230] The lateral width Wd of the laterally flared distal end
portion increases along the distal end portion 3220 toward the
proximal end portion 3260. In some embodiments, without limitation,
lateral width Wd of the laterally flared distal end portion
increases by a total of between about 0.2 mm to about 1.2 mm, or
about 0.3 mm to about 1.0 mm, or about 0.4 mm to about 0.9 mm, or
about 0.5 mm to about 0.8 mm, or about 0.5 mm to about 0.7 mm.
[0231] Mid-body portion 3240 extends between proximal portion 3260
and distal portion 3220. Mid-body portion 3240 has a lateral width
Wm. In the depicted embodiment, lateral width Wm is laterally
narrower than some portions of each proximal portion 3260 and
distal portion 3220. In some embodiments, a maximum lateral width
Wm is at least about 0.3 mm less than a maximum lateral width Wd.
In some embodiments, without limitation, a maximum lateral width Wm
is at least about 0.1 mm less, or about 0.2 mm less, or about 0.4
mm less, or about 0.5 mm less, or about 0.6 mm less, or about 0.8
mm less, or about 1.0 mm less, or about 1.2 mm less than a maximum
lateral width Wd.
[0232] In some embodiments, maximum lateral width Wm is at least
about 0.5 mm less than a maximum lateral width Wp of proximal
portion 3260. In some embodiments, without limitation, a maximum
lateral width Wm is at least about 0.1 mm less, or about 0.2 mm
less, or about 0.3 mm less, or about 0.4 mm less, or about 0.6 mm
less, or about 0.7 mm less, or about 0.8 mm less, or about 0.9 mm
less, or about 1.0 mm less, or about 1.2 mm, or about 1.4 mm less
than a maximum lateral width Wp.
[0233] In the depicted embodiment, mid-body portion 3240 includes a
plurality of lateral protrusions 3242. Such lateral protrusions
3242 can improve the anchoring strength of device 3200 to tissue,
and thereby help facilitate migration resistance of device 3200. In
some embodiments, such as the depicted embodiment, at least some
edges of lateral protrusions 3242 extend laterally along angles
that are non-orthogonal in relation to longitudinal axis 3201. In
some embodiments, without limitation, edges of lateral protrusions
3242 can extend laterally along angles between about 0 degrees to
about 80 degrees, or about 10 degrees to about 80 degrees, or about
30 degrees to about 80 degrees, or about 40 degrees and about 70
degrees, or about 50 degrees and about 70 degrees, or about 40
degrees and about 60 degrees in relation to the longitudinal axis
3201.
[0234] One or more portions of external surface 3210 can be
configured for enhanced friction with eye tissue (e.g., the cornea
or sclera). Advantageous mechanical stability and/or migration
resistance of the device 3200 (and the other devices provided
herein) in relation to the eye can be facilitated by such portions.
For example, in the depicted embodiment, a surface portion 3218
includes an enhanced texture (roughness) in comparison to other
portions of external surface 3210. In the depicted embodiment,
surface portion 3218 is a waffled surface (cross-hatched
engravings). In some embodiments, other types of texturing
configurations can be alternatively or additionally included. For
example, such texturing configurations can include, but are not
limited to, etching, stippling, knurling, inclusion of one or more
barbs, and the like, and combinations thereof. In some embodiments,
the surface portion 3218 is created by techniques such as, but not
limited to, laser machining, chemical etching, plasma etching, 3D
printing, photo etching, and the like.
[0235] In the depicted embodiment, proximal end portion 3260
includes a radiused proximal edge 3262 having a radius 3264, a
first lateral edge 3266, and a second lateral edge 3268. Radiused
proximal edge 3262 extends along an arc between first lateral edge
3266 and second lateral edge 3268. In some cases, a radiused
proximal edge 3262 can facilitate a uniform projection of device
3200 from an eye surface as compared to a non-radiused distal
leading edge.
[0236] In the depicted embodiment, radius 3264 is centered on axis
3201 such that body 3203 is symmetrical about axis 3201, but such
centering and axial symmetry is not required in all embodiments. In
some embodiments, radius 3264 is between about 5.0 mm and about
10.0 mm. In some embodiments, without limitation, radius 3264 is
between about 3.0 mm and about 12.0 mm, or about 4.0 mm and about
11.0 mm, or about 6.0 mm and about 9.0 mm, or about 7.0 mm and
about 8.0 mm.
[0237] Proximal end portion 3260 also includes radiused distal
edges 3270a and 3270b. Radiused distal edges 3270a and 3270b can
abut an outer surface of an eye when device 3200 is implanted in
the eye. In some embodiments, radiused distal edges 3270a and 3270b
have radii between about 5.0 mm and about 10.0 mm. In some
embodiments, without limitation, radiused distal edges 3270a and
3270b have radii between about 3.0 mm and about 12.0 mm, or about
4.0 mm and about 11.0 mm, or about 6.0 mm and about 9.0 mm, or
about 7.0 mm and about 8.0 mm.
[0238] In some embodiments, maximum longitudinal length L of body
3203 in comparison to a maximum lateral width (Wp in the depicted
embodiment) of body 3203 is a ratio between about 1:1 to about 3:1.
In some embodiments, without limitation, maximum longitudinal
length L of body 3203 in comparison to a maximum lateral width of
body 3203 is a ratio between about 1:1 to about 2.5:1, or about 1:1
to about 2:1, or about 1.3:1 to about 1.8:1, or about 1.6:1 to
about 2.2:1.
[0239] Referring to FIGS. 44 and 45, another example device 3300 in
accordance with some embodiments provided herein is illustrated.
Device 3300 includes a body 3303 that defines a lumen 3305 and a
longitudinal axis 3301. Body 3303 includes a distal end portion
3320, a mid-body portion 3340, and a proximal end portion 3360.
Body 3303 includes a distal edge 3322 and a proximal edge 3362.
Body 3303 has an external surface 3310 and a lumenal surface
3312.
[0240] Device 3300 is structurally configured essentially like
device 3200. One difference between devices 3300 and 3200 is that
device 3300 includes a surface portion 3318 that has been roughened
by an oxygen plasma etching process. In the depicted embodiment,
the roughened surface portion 3318 is on the mid-body portion 3340
only. In some embodiments, other portions of body 3303 may
alternatively or additionally have roughened surface portions 3318
from an oxygen plasma etching process. Any of the device
embodiments described herein can include one or more roughened
surface portions that are created by any of the processes described
herein, including, but not limited to, oxygen plasma etching.
[0241] Referring to FIGS. 46 and 47, another example device 3400 in
accordance with some embodiments provided herein is illustrated.
Device 3400 includes a body 3403 that defines a lumen 3405 and a
longitudinal axis 3401. Body 3403 includes a distal end portion
3420, a mid-body portion 3440, and a proximal end portion 3460.
Body 3403 includes a distal edge 3422 and a proximal edge 3462.
Body 3403 has an external surface 3410, a lumenal surface 3412, and
a surface portion 3418 that has been roughened, for example by an
oxygen plasma etching process.
[0242] Device 3400 is structurally configured essentially like
device 3200. One difference between devices 3400 and 3200 is that
device 3400 includes suture attachment structures 3466a and 3466b
that are defined in proximal end portion 3460. The suture
attachment structures 3466a and 3466b are V-grooves in the depicted
embodiment. In some embodiments, other types of suture attachment
structures can be alternatively or additionally included (e.g.,
slots, eyelets, notches, etc.). While the depicted embodiment
includes two suture attachment structures 3466a and 3466b, in some
embodiments, zero, one, three, four, or more than four suture
attachment structures are included.
[0243] Referring to FIGS. 48 and 49, another example device 3500 in
accordance with some embodiments provided herein is illustrated.
Device 3500 includes a body 3503 that defines a first lumen 3505, a
second lumen 3506, and a longitudinal axis 3501. Body 3503 includes
a distal end portion 3520, a mid-body portion 3540, and a proximal
end portion 3560. Body 3503 includes a distal edge 3522 and a
proximal edge 3462. Body 3503 has an external surface 3510, a first
lumenal surface 3512, and a second lumenal surface 3513.
[0244] Body 3503 also defines an opening 3580. That is, mid-body
portion 3540 comprises two longitudinal portions that are spaced
apart from each other to thereby define opening 3580 in between
each other. The two longitudinal portions converge at the distal
end of the mid-body portion 3540 to attach to the single distal end
portion 3520. At the proximal end of the mid-body portion 3540, the
two longitudinal branch portions attach to the proximal end portion
3560 at two distinct places, respectively. Opening 3580 can
advantageously provide an opening space for tissue (e.g., sclera
tissue) to grow into and through, so that body 3503 becomes
encapsulated and secure as a result of the tissue ingrowth.
[0245] Device 3500 can also include one or more other features
shown in the context of other device embodiments described herein.
For example, without limitation, device 3500 can include features
such as, but not limited to, suture attachment structures,
roughened surface portions, and lateral protrusions.
[0246] Referring to FIGS. 50 and 51, another example device 3600 in
accordance with some embodiments provided herein is illustrated.
Device 3600 includes a body 3603 that defines a lumen 3605. Body
3603 includes a distal end portion 3620, a mid-body portion 3640,
and a proximal end portion 3660. Body 3603 includes a distal edge
3622 and a proximal edge 3662. Body 3603 has an external surface
3610 and a surface portion 3618 that has been roughened, for
example by an oxygen plasma etching process. Device 3600 includes
suture attachment structures 3666a and 3666b that are defined in
proximal end portion 3660. The suture attachment structures 3666a
and 3666b are V-grooves in the depicted embodiment. In some
embodiments, other types of suture attachment structures can be
alternatively or additionally included (e.g., slots, eyelets,
notches, etc.). While the depicted embodiment includes two suture
attachment structures 3666a and 3666b, in some embodiments, zero,
one, three, four, or more than four suture attachment structures
are included.
[0247] Device 3600 is structurally configured essentially like
device 3400. One difference between devices 3600 and 3400 is that
device 3600 defines a first chamber 3624a and a second chamber
3624b. Chambers 3624a-b are sealed spaces that are located in
distal end portion 3620 on opposite sides of lumen 3605. Each of
the chambers 3624a-b is separated from lumen 3605 by a thin,
deflectable polymer wall (e.g., made of anti-biofouling PEG).
Chambers 3624a-b can be filled with a gas such as air, nitrogen,
CO2, or another type of gas. Since gas-filled chambers 3624a-b can
be considered to follow the ideal gas law (PV=nRT, where nRT is
constant), the change in pressure within lumen 3605 is accompanied
by a corresponding change in the volume of gas within chambers
3624a-b. For example, as depicted in FIG. 51 (in comparison to FIG.
50), the thin membrane wall separating chambers 3624a-b from lumen
3605 will deflect into/towards lumen 3605 in response to a pressure
decrease in lumen 3605. This partial occlusion of lumen 3605
results in an increased resistance to flow through lumen 3605
(e.g., preventing or inhibiting hypotony). Alternatively, with
increasing IOP, lumen 3605 will become more opened as shown in FIG.
50 for example (compared to FIG. 51), allowing greater flow through
lumen 3605 in patients with very high IOP.
[0248] Referring to FIGS. 52 and 53, in some cases an example
insertion tool 3700 can be used to puncture a patient's sclera and
to deploy an implant device 3750 in essentially a single step. A
distal end portion of insertion tool 3700 is depicted (FIG. 52 is a
plan view and FIG. 53 is a side view). A handle of any suitable
style may be coupled to the depicted distal end portion of
insertion tool 3700. Implant device 3750 is representative of any
of the implant devices described herein.
[0249] Insertion tool 3700 includes a first, distal-most blade
member 3710 and a second blade member 3720 that does not extend as
far distally as distal-most blade member 3710. The blade members in
some ways resemble keratome ophthalmic blades. The blade members
3710 and 3720 are coupled together such that a slot is defined
between distal-most blade member 3710 and second blade member 3720.
The slot is longer than the implant device 3750.
[0250] Implant device 3750 can be releasably received in the slot
between blade members 3710 and 3720. Distal-most blade member 3710
extends farther distally than second blade member 3720.
Accordingly, in use, as insertion tool 3700 is advanced toward an
eye, distal-most blade member 3710 will be the first to pierce the
tissue (e.g., scleral tissue). As insertion tool 3700 is advanced
further distally, second blade member 3720 will subsequently pierce
the tissue. As insertion tool 3700 is advanced still further
distally, implant device 3750 will be positioned within the
confines of the eye tissue until a proximal end portion 3752 of
implant device 3750 abuts the outer surface of the eye. Then,
insertion tool 3700 can be withdrawn (leaving implant device 3750
within the eye except for the protruding proximal end portion
3752). In some cases, another tool can be used to stabilize implant
device 3720 as insertion tool 3700 is withdrawn. In some
embodiments, insertion tool 3700 includes an implant device
ejection actuator that can be actuated to press implant device 3750
out of the slot between blade members 3710 and 3720 while insertion
tool 3700 is being withdrawn.
[0251] It should be understood that one or more features from one
or more devices described herein can be combined with one or more
features from one or more other devices described herein. All such
combinations and permutations are within the scope of this
disclosure.
[0252] While this specification contains many specific
implementation details, these should not be construed as
limitations on the scope of any invention or of what may be
claimed, but rather as descriptions of features that may be
specific to particular embodiments of particular inventions.
Certain features that are described in this specification in the
context of separate embodiments can also be implemented in
combination in a single embodiment. Conversely, various features
that are described in the context of a single embodiment can also
be implemented in multiple embodiments separately or in any
suitable subcombination. Moreover, although features may be
described herein as acting in certain combinations and even
initially claimed as such, one or more features from a claimed
combination can in some cases be excised from the combination, and
the claimed combination may be directed to a subcombination or
variation of a subcombination.
[0253] Similarly, while operations are depicted in the drawings in
a particular order, this should not be understood as requiring that
such operations be performed in the particular order shown or in
sequential order, or that all illustrated operations be performed,
to achieve desirable results. In certain circumstances,
multitasking and parallel processing may be advantageous. Moreover,
the separation of various system modules and components in the
embodiments described herein should not be understood as requiring
such separation in all embodiments, and it should be understood
that the described program components and systems can generally be
integrated together in a single product or packaged into multiple
products.
[0254] Particular embodiments of the subject matter have been
described. Other embodiments are within the scope of the following
claims. For example, the actions recited in the claims can be
performed in a different order and still achieve desirable results.
As one example, the processes depicted in the accompanying figures
do not necessarily require the particular order shown, or
sequential order, to achieve desirable results. In certain
implementations, multitasking and parallel processing may be
advantageous.
* * * * *